Dole Salad Blends Recalled

Dole Fresh Vegetables Recalls Bagged Salads Due to Possible Health Risk

 March 13, 2014 - Dole Fresh Vegetables is voluntarily recalling a limited number of cases of bagged salad. The products being recalled are Dole Italian Blend (UPC 7143000819), Fresh Selections Italian Style Blend (UPC 1111091045), Little Salad Bar Italian Salad (UPC 4149811014) and Marketside Italian Style Salad (UPC 8113102780) coded A058201A or B, with Use-by date of March 12, 2014 due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.

 The product code and Use-by date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in 15 U.S. states (Connecticut, Florida, Illinois, Indiana, Kentucky, Maryland, Massachusetts, Michigan, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Virginia) and 3 Canadian provinces (New Brunswick, Ontario & Quebec).

No illnesses have been reported in association with the recall. This precautionary recall notification is being issued due one sample of Dole Italian salad which yielded a positive result for Listeria monocytogenes in a random sample test conducted by the Canadian Food Inspection Agency.

Although product is 1 day past its Use-By date and it is highly unlikely that any product is still available at retail, retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is being removed from the stream of commerce.

Listeria monocytogenes is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.

No other salads are included in the recall. Only the specific Product Codes, UPC codes and March 12, 2014 Use-by date identified above are included in the recall. Consumers who have any remaining product with these Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 am to 3:00 pm (PT) Monday - Friday.

Contact:
Consumer:
800-356-3111
Media:
William Goldfield
818-874-4647
William.Goldfield@Dole.com

MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All Weight Loss Formulas

Recalled weight-loss products include:

• Magic Slim
• Fruta Bio
• SlimEasy
• Super Fat Burning Bomb
• Slim Xtreme
• Meizi Evolution
• Meizitang Strong Version Botanical Slimming
• Jianfeijindan Activity Girl
• Japan Hokkaido Cangye Pharmacy Co., LTD: Japanese & Chinese Formula pill for weight reduction

Contact:
MyNicKnaxs, LLC
386-337-8142

FOR IMMEDIATE RELEASE- February 4, 2014 - MyNicKnaxs, LLC., located in Florida is announcing a recall of: Magic Slim, Fruta Bio, SlimEasy, Super Fat Burning Bomb, Slim Xtreme, Meizi Evolution, Meizitang Strong Version Botanical Slimming, Jianfeijindan Activity Girl, and Japan Hokkaido Cangye Phamacy Co., LTD Japanese Chinese Formula pill for weight reduction because these products contain undeclared active pharmaceutical ingredients: Phenolphthalein, sibutramine or a combination of both. At this time no illnesses or injuries have been reported to MyKnicKnaxs, LLC., in connection with these products.

Phenolphthalein was once an ingredient used in over-the-counter laxatives, but because of concerns of carcinogenicity is not currently approved for marketing in the United States. Sibutramine is an appetite suppressant (drug Schedule IV) that was withdrawn from the U.S. market in October 2010 for safety reason (seizure, cardiovascular risks: heart attacks, arrhythmia and strokes among others). These undeclared ingredients makes these products unapproved new drugs for which safety and efficacy have not been established. Consumption of this product could include potentially serious gastrointestinal disturbances, irregular heartbeat, and cancer with long-term use.

All lots of these products are being recalled.

MyKnicKnaxs, LLC. has taken this voluntary action because it is committed to providing accurate information to all customers and is concerned for the health and safety of all users . MyKnicKnaxs, LLC, is working with the FDA in the recall process. We sincerely regret any inconvenience the recall may cause customers.

Customers are advised to immediately discontinue use and should return the products immediately to the place of purchase. Consumers with questions should contact Chevonne Torres at 386-337-8142 or via e-mail at nicnaxs@yahoo.com Monday - Friday,2:00 am – 7:00 pm, EDT.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Online: www.fda.gov/medwatch/report.htm
• Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm Mail to address on the pre-addressed form.
• Fax: 1-800-FDA-0178

Tomatoes Recalled in Florida Due to Salmonella Risk

Big Red Tomato Packers, LLC Voluntarily Recalls Fresh Tomatoes Due to Possible Risk of Contamination from Salmonella 

Consumer Contact:
772-466-0700

FOR IMMEDIATE RELEASE - February 7, 2014 - Big Red Tomato Packers, LLC of Fort Pierce, FL is voluntarily issuing a limited recall of 790 - 20 and 25 lb. boxes of fresh tomatoes of lot 1106, because they may have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting or abdominal pain.

This is a voluntary precautionary recall as there are no known illnesses associated with this lot number.

Tomatoes from the lot were distributed to a limited number of receivers in Florida, North Carolina, Michigan, Minnesota, Pennsylvania and Tennessee. All receivers of the lot have been notified.

The potential for contamination was discovered as the result of a routine random lot sample taken on January 28, 2014. All currently existing product associated with this lot number is subject to this recall.

Big Red Tomato Packers is and will remain committed to being a quality producer of Florida tomatoes. Big Red is currently reviewing all policies and procedures associated with food safety to minimize any future occurrence.

Any product remaining in the market channels should be disposed of immediately.

For more information, please contact Erin Cox at 772-466-0700 or erin@bigredtomatopackers.com

WARNING: Uncle Ben's Infused Rice - All Lot Numbers Recalled in Texas

FDA warns against using Uncle Ben’s Infused Rice

Mars Foodservices recalls all lot numbers of Infused Rice linked to recent illness in Texas 

For Immediate Release: Feb. 10, 2014
Media Inquiries: Theresa Eisenman, 301-796-2805, theresa.eisenman@fda.hhs.gov

Consumer Inquiries: 1-888-INFO-FDA 

Fast Facts:

• Government officials are investigating a cluster of illnesses associated with Uncle Ben’s Infused Rice Mexican Flavor sold in 5- and 25-pound bags.
• Out of an abundance of caution, the FDA is warning food service companies and consumers not to use any Uncle Ben’s Infused Rice products sold in 5- and 25-pound bags.
• These products are sold to food service companies that typically distribute to restaurants, schools, hospitals and other commercial establishments. However, the products may be available over the Internet and at warehouse-type retailers. 
• Food service companies and consumers who have purchased the products should not use the rice, and should return it to their point of purchase or dispose of it.     
• Uncle Ben’s Brand Ready to Heat, Boxed, Bag or Cup products sold at grocery stores and other retail outlets are not being recalled.

What is the Problem and What is Being Done about the Problem?

The FDA, the Centers for Disease Control and Prevention (CDC), and state and local officials have been investigating a cluster of illnesses associated with Uncle Ben’s Infused Rice Mexican Flavor sold in 5- and 25-pound bags. 

On Feb. 7, 2014, the FDA’s Coordinated Outbreak Response and Evaluation Network (CORE) was notified of a cluster of illnesses at three public schools in Katy, Texas. Thirty-four students and four teachers experienced burning, itching rashes, headaches and nausea for 30 to 90 minutes, before the symptoms went away. Uncle Ben’s Infused Rice Mexican Flavor with the lot number 351EKGRV01, made by Mars Foodservices of Greenville, Miss., was the common food item eaten by ill students.

On Dec. 4, 2013, the Illinois Department of Public Health notified CDC of 25 children with similar skin reactions following a school lunch that served an Uncle Ben’s Infused Rice product. North Dakota reported a similar incident that occurred on Oct. 30, 2013. Three children in a daycare and one college student experienced flushing reactions 45 minutes after consuming an Uncle Ben’s Infused Rice product.

Mars Foodservices is recalling all bags and all lot numbers of its Uncle Ben’s Infused Rice products produced in 2013: 

• UNCLE BEN’S INFUSED Rice Roasted Chicken Flavor (5- and 25-pounds)
• UNCLE BEN’S INFUSED Rice Garlic & Butter Flavor (5-pounds)
• UNCLE BEN’S INFUSED Rice Mexican Flavor (5- and 25-pounds)
• UNCLE BEN’S INFUSED Rice Pilaf (5-pounds)
• UNCLE BEN’S INFUSED Rice Saffron Flavor (5-pounds)
• UNCLE BEN’S INFUSED Rice Cheese Flavor (5-pounds)
• UNCLE BEN'S INFUSED Rice Spanish Flavor (25-pounds)

Although this product is not typically marketed to individual consumers, it may be available over the Internet and at warehouse-type retailers.

Uncle Ben’s Brand Ready to Heat, Boxed, Bag or Cup products sold at grocery stores and other retail outlets are not being recalled.

Investigation into this outbreak continues. 

What are the Symptoms of Illness/Injury? 
The symptoms associated with this illness include a red burning/itching rash, headache, nausea, and flushness of the skin.

The symptoms appear very shortly after consuming the rice product and pass within 30 to 90 minutes.

What Specific Products are being Recalled? 

Mars Foodservices is recalling all bags and all lot numbers of its Uncle Ben’s Infused Rice products produced in 2013:

• UNCLE BEN’S INFUSED Rice Roasted Chicken Flavor (5- and 25-pounds)
• UNCLE BEN’S INFUSED Rice Garlic & Butter Flavor (5-pounds)
• UNCLE BEN’S INFUSED Rice Mexican Flavor (5- and 25-pounds)
• UNCLE BEN’S INFUSED Rice Pilaf (5-pounds)
• UNCLE BEN’S INFUSED Rice Saffron Flavor (5-pounds)
• UNCLE BEN’S INFUSED Rice Cheese Flavor (5-pounds)
• UNCLE BEN'S INFUSED Rice Spanish Flavor (25-pounds)

The products are sold to food service companies. However, they may be available over the Internet and at warehouse-type retailers. 

Who is at Risk?

People of any age can experience symptoms. The illnesses in Texas included people of different ages (children and adults).

What Do Food Service Companies and Consumers Need To Do? 
Food service companies and consumers who may have purchased the products should not use the rice, and should return it to their distributor or point of purchase or dispose of it. 

What Does the Product Look Like?

Photos of Uncle Ben’s Infused Rice products can be seen here: https://www.marsfoodservices.com/products-brands/uncle-bens-rice-and-beans/infused-rice.aspx.

Where is it Distributed?

The products are sold directly to food service companies that typically distribute to restaurants, schools, hospitals and other establishments. The products have also been found over the Internet, including Amazon and warehouse-type retailers, such as Sam’s Club.

Who Should be Contacted? 
Contact your health care provider if you have sudden nausea, headaches or a burning/itching rash after eating Uncle Ben’s Infused Rice products.

The FDA encourages consumers with questions about food safety to call 1-888-SAFEFOOD Monday through Friday between 10 a.m. and 4 p.m. eastern time, or to consult the fda.gov website:http://www.fda.gov/Safety/ReportaProblem/ConsumerComplaintCoordinators/default.htm.

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.

# # #

Avastin Eye Medicine Recalled

Avastin Unit Dose Syringes by Clinical Specialties

Recalled: Potential For Serious Eye Infection

Avastin Eye Injection

AUDIENCE: Eye Care Health Professionals, Patients

THE ISSUE

Clinical Specialties is voluntarily recalling Avastin unit dose syringes. The product has or potentially could result in an infection within the eye. Clinical Specialties has received reports of five intra-ocular infections from physician’s office and this is how the problem was identified.

BACKGROUND

This product was being used solely as an off label use by an ophthalmologist for macular degeneration and is packaged in sterile syringes (see Press Release for a list of lot numbers). This product would be administered by a licensed physician in a surgery or physician’s office setting and syringes were distributed to doctors’ offices in Georgia, Louisiana, South Carolina, and Indiana from December 18, 2012 to present.

RECOMMENDATION

Doctors that have product which is being recalled should stop using the Avastin immediately. Consumers with questions regarding this recall may contact Clinical Specialties by phone at 866-880-1915 or e-mail address at clinicalrx@bellsouth.net Monday through Friday between the hours of 10 am to 5 pm EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Warning: Antibiotic Azithromycin May Cause Fatal Heart Rhythms

Azithromycin (Zithromax or Zmax): Risk of Potentially Fatal Heart Rhythms

AUDIENCE: Family Practice, Patient, Pharmacy, Health Professional

Click on this video to view other brand names of this drug.

ISSUE: FDA is warning the public that azithromycin (Zithromax or Zmax) can cause abnormal changes in the electrical activity of the heart that may lead to a potentially fatal irregular heart rhythm. Patients at particular risk for developing this condition include those with known risk factors such as existing QT interval prolongation, low blood levels of potassium or magnesium, a slower than normal heart rate, or use of certain drugs used to treat abnormal heart rhythms, or arrhythmias.  FDA has issued a Drug Safety Communication today as a result of our review of a study by medical researchers as well as another study by a manufacturer of the drug that assessed the potential for azithromycin to cause abnormal changes in the electrical activity of the heart.

FDA previously released a Statement on May 17, 2012, about a study that compared the risks of cardiovascular death in patients treated with the antibacterial drugs azithromycin, amoxicillin, ciprofloxacin (Cipro), and levofloxacin (Levaquin), or no antibacterial drug. The study reported an increase in cardiovascular deaths, and in the risk of death from any cause, in persons treated with a 5-day course of azithromycin (Zithromax) compared to persons treated with amoxicillin, ciprofloxacin, or no drug. The risks of cardiovascular death associated with levofloxacin treatment were similar to those associated with azithromycin treatment.

BACKGROUND: Azithromycin is marketed under the brand names Zithromax and Zmax. Change to “FDA-approved indications for azithromycin include: acute bacterial exacerbations of chronic obstructive pulmonary disease, acute bacterial sinusitis, community-acquired pneumonia, pharyngitis/tonsillitis, uncomplicated skin and skin structure infections, urethritis and cervicitis, genital ulcer disease

RECOMMENDATION: Health care professionals should consider the risk of torsades de pointes and fatal heart rhythms with azithromycin when considering treatment options for patients who are already at risk for cardiovascular events.  FDA notes that the potential risk of QT prolongation with azithromycin should be placed in appropriate context when choosing an antibacterial drug: Alternative drugs in the macrolide class, or non-macrolides such as the fluoroquinolones, also have the potential for QT prolongation or other significant side effects that should be considered when choosing an antibacterial drug.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

• Complete and submit the report Online: www.fda.gov/MedWatch/report.htm
• Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

Read the complete MedWatch Safety Alert, including a link to the Drug Safety Communication, at:

http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm343350.htm

Night Bullet, Male Sexual Performance Supplement Recalled

Green Planet, Inc. Issues a Voluntary Nationwide Recall 

of One Lot of "Night Bullet" 

Marketed as a Supplement to Support Male Sexual Performance

Contains Undeclared, Potentially Hazardous Active Ingredient

March 11, 2013 - Green Planet, Inc. is conducting a voluntary consumer recall of a product sold as a dietary supplement under the brand name of "Night Bullet," found to contain trace amounts of an analogue of an FDA-approved drug.

Finished product of Night Bullet was tested and found to contain trace amounts of an analogue of an FDA-approved drug. Analytical tests conducted by the Food and Drug Administration (FDA) of Night Bullet found that the product contains trace amounts of Sulfohydroxyhomosildenafil and Aminotadalafil. Sulfohydroxyhomosildenafil and Aminotadalafil are an analogues of sildenafil. Sildenafil is the active pharmaceutical ingredient in an FDA-approved drug that is used to treat erectile dysfunction (ED) making this product an unapproved drug.

These undeclared active ingredients pose a threat to consumers because sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates. ED is a common problem in men with these conditions and they may seek products to enhance sexual performance. Additionally sildenafil may cause side effects such as, headaches and flushing. Green Planet has not received any reports of adverse events related to this recall.

Night Bullet is marketed as a supplement for male enhancement. The recalled products are in capsule form, packaged in one (1) count blister packs. The lot and expiration date can be found on the back of the package. The following lot is being recalled:

Product:  Night Bullet

Batch Lot #:  B43N032

UPC Code:  018505122233

Expiration Date:  10/20/15

Night Bullet was sold nationwide between October 2012 and March 2013 to wholesalers and sample provided at trade shows.

Green Planet is notifying its wholesalers through written correspondence. We urge consumers who have purchased these products to immediately discontinue their use and contact their physician if they have experienced any problems that may be related to taking this product. The Company is advising consumers to return the product to their place of purchase. Consumers may also return products directly to Freedom Trading. Customers can call the Company at 877-621-2048 Monday through Friday from 9:00 am – 5:00 pm PST for instructions on the return and refund process.

Any adverse events or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting Program either online, by regular mail or by fax:

• Online: http://www.fda.gov/medwatch/report.htm
• Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at:
  http://www.fda.gov/MedWatch/getforms.htm. Mail to address on the preaddressed form.
• Fax: 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Contacts

Consumer:s:

877-621-2048

contact@thegreenplanetproducts.com

Premium Cat Food Recalled: Low Levels of Vitamin B1

Premium Edge, Diamond Naturals and 4health Dry Cat Food Formulas Voluntarily Recalled Due to Possibility of Low Levels of Thiamine (Vitamin B1)

March 10, 2013 - COLUMBIA, S.C. - Diamond Pet Foods is voluntarily recalling limited production codes of Premium Edge Finicky Adult Cat Formula dry cat food, Premium Edge Senior Cat Hairball Management Formula dry cat food, Premium Edge Kitten Formula dry cat food, Diamond Naturals Kitten Formula dry cat food and 4health All Life Stages Cat Formula dry cat food. Tests conducted by the company indicated the products might have a low level of thiamine (Vitamin B1). There have been no complaints regarding thiamine levels, or any other health issues, related to these products. In association with this voluntary recall, Diamond Pet Foods has tested all other Diamond brands for thiamine deficiency to ensure the safety of the cat food it manufactures. No other product manufactured by Diamond Pet Foods is involved in this voluntary recall.

Only product with the following Best By dates and Production Codes are included in the voluntary recall. Further distribution of these affected production codes has occurred through online sales. It is best to check the production code to determine if the product has been recalled or not.

Product	Size	Production Codes	Best By
Premium Edge Finicky Adult Cat Formula	18 lb. bags	NGF0703	10-Jul-2013
Premium Edge Finicky Adult Cat Formula	6 lb. bags	NGF0802	15-Aug-2013, 16-Aug-2013
Premium Edge Senior Cat Hairball Management Formula	6 lb. and 18 lb. bags	NGS0101	03-Jan-2014, 04-Jan-2014
Premium Edge Senior Cat Hairball Management Formula	6 lb. and 18 lb. bags	NGS0702	10-Jul-2013
Premium Edge Kitten Formula	6 oz. samples, 6 lb. and 18 lb. bags	MKT0901	26-Sept-2013 29-Sept-2013 30-Sept-2013 02-Oct-2013
Diamond Naturals Kitten Formula	6 oz. samples and 6 lb. bags	MKT0901	30-Sept-2013
4health All Life Stages Cat Formula	5 lb. and 18 lb. bags	NGF0802	14-Aug-2013, 18-Aug-2013

"At Diamond Pet Foods, we have a process where we continuously test our products, and this process allowed us to find the undesired levels of thiamine in some of our cat formulas. Our food safety protocols are designed to provide safe food on a daily basis," says Michele Evans, Ph.D., Diamond Pet Foods Executive Director of Food Safety and Quality Assurance. "In the event an error occurs, we have the data to quickly alert pet owners, giving them the confidence they demand of a pet food manufacturer."

Pet owners who are unsure if the product they purchased is included in the recall, or who would like replacement product or a refund, may contact the Pet Food Information Center at 1­888­965­6131, Sunday through Saturday, 8 a.m. – 6 p.m. EST. Consumers also may visit Website - http://www.petfoodinformationcenter.com for additional information.

Cats fed product with the previously listed Production Codes and Best By dates exclusively for several weeks may be at risk for developing a thiamine deficiency. Thiamine is essential for cats in maintaining normal nervous system function. Symptoms of thiamine deficiency displayed by an affected cat can be gastrointestinal or neurological in nature. Early signs of thiamine deficiency may include decreased appetite, salivation, vomiting and weight loss. In advanced cases, neurological signs can develop, which may include ventriflexion (bending towards the floor) of the neck, wobbly walking, falling, circling and seizures. Pet owners should contact their veterinarians immediately if a cat is displaying any of these signs. If treated promptly, thiamine deficiency typically is reversible.

Contacts

Consumers:

888-965-6131

Media:

877-274-7391

Dog and Cat Foods Might Pose Danger to Your Health

How to Protect Your Family From Food-borne Illness in Your Pet's Foods

Recently, I've noticed that more and more recalls have been issued for pet foods due to contamination with dangerous bacteria such as salmonella and e. coli.  Not only do these foods pose a danger to your beloved pets, but they also are a hazard to you and your family!  While salmonella in pet foods and treats can cause serious infections in your dog or cat, they can cause very real problems in people too--especially children, the elderly, and people with compromised immune systems. 

Salmonella in pet foods and treats potentially can be transferred to people ingesting or handling the contaminated products.Toddlers are notorious for messing around with pets' dishes and (as unsavory as it sounds) they sometimes will even eat the dog or cat's food.  But even if you keep pet food well away from your little ones, you might still be at risk of contracting a serious infection due hidden bacteria in your animals' foods.  Luckily, there are steps you can take  to help prevent these food-borne illnesses that arise from pet food contamination..  Following the guidelines listed below will go a long way toward protecting your family and your fur-babies as well.

When Buying Pet Food

• Purchase products that appear to be in good condition, without signs of damage to the packaging such as dents or tears.

When Preparing Pet Food

• Thoroughly wash your hands for 30 seconds with hot soapy water after handling pet foods and treats.
• Wash pet food bowls, dishes, and scooping utensils with soap and hot water after each use.
• Do not use your hands or the pet's feeding bowl as a scooping utensil—use a clean, dedicated scoop or spoon.
• Dispose of old or spoiled pet food products in a safe manner, such as in a securely tied plastic bag in a covered trash receptacle.

Safely Storing Pet Food

• Securely cover and refrigerate promptly or discard any unused, leftover wet pet food.
• Refrigerators should be set at or below 40º F.
• Dry products should be stored in a cool, dry place—under 80º F.
• If possible, store dry pet food in its original bag inside a clean, dedicated plastic container with a lid, keeping the top of the bag folded closed.
• Keep pets away from food storage and preparation areas.
• Keep pets away from garbage and household trash.

Stay Alert

• Finally, stay alert to breaking news on product recalls by subscribing to Totally Recalled!  where you will always find  timely updates to help you avoid exposure to any known problems as they occur--such as this pet treat recall issued today!  

"Diggin' Your Dog" Dog Treats Recalled Due to Salmonella

Diggin' Your Dog Recalls Strippin' Chicks Pet Treats Distributed in Colorado and Nevada Due to Possible Salmonella Hazard

March 7, 2013 - Diggin' Your Dog™ announced today that they are voluntarily withdrawing one lot of its Strippin' Chicks™ Pet Treats produced on 8-30-12 because they have the potential to be contaminated with Salmonella. The sample was obtained in Colorado and the company has accounted for its distribution in Colorado of this lot.

No other Diggin' Your Dog™ products, lots, or production dates are affected.

The lot being voluntarily withdrawn is: Strippin' Chicks™ Pet Treats 5 oz Bag. Lot Code 250322 Use By Date: 2-23-14.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Animals with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some animals will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy animals can be carriers and infect other animals or humans. If your animals have consumed the recalled product and have these symptoms, please contact your veterinarian.

Diggin' Your Dog™ takes the matter of consumer protection and safety very seriously and strives to deliver only the safest products available.

Diggin' Your Dog™ is committed to providing the highest-quality pet treats possible to their customers. As a precautionary measure, Diggin' Your Dog™ will continue to produce all products in very small, handmade lot batches.

No Other Diggin' Your Dog™ products are affected by this voluntary withdrawal. Customers who have purchased this lot code are urged to stop feeding the product to their pet, remove the lot code from the packaging, and discard the contents.

A full refund, plus $1.00 to cover postage will be received by mailing the UPC and lot code to:
Diggin Your Dog, LLC, PO Box 17306 Reno, NV 89511.
All refunds will be processed within ten business days (plus postage time).

Diggin' Your Dog™ values the efforts of all agencies dedicated to the safety of the industry and is committed to consumer safety at all levels.

For questions or more information, contact Diggin' Your Dog™.
By phone at 775-742-7295 Mon-Fri 8:30AM - 4:00PM Pacific Standard Time
Email us at info@dydusa.com.

Chicken of the Sea Tuna Recalled, Poorly Sealed Cans

Tri-Union Seafood Issues Voluntary Recall on Select 5-Ounce Chunk White Albacore Tuna in Water

FOR IMMEDIATE RELEASE - Mar. 6, 2013 – Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken of the Sea brand 5-ounce cans of chunk white albacore tuna in water.

The seams on the lids of the cans do not meet the standard for seam quality. Cans that do not meet seam standards could result in product contamination by spoilage organisms or by pathogens, which could lead to illness if consumed. There have been no reported illnesses to date, and Tri-Union Seafoods is issuing this voluntary recall to ensure the highest margin of safety and quality.

The specific product being recalled is Chicken of the Sea Brand 5-ounce chunk white albacore tuna in water sold at retail nationwide in single cans between February 4, 2013 and February 27, 2013.

The UPC code (also known as the bar code) is found on the label of the product and is 0 48000 03355 0. The Best By date is printed on the bottom of the can and is 01/18/17. The product lot codes that are part of this voluntary recall can also be found on the bottom of the can and include:

CODE	BEST BY DATE
3018CACCKP	01/18/17
3018CAECKP	01/18/17
3018CB3CKP	01/18/17
3018CADCKP	01/18/17

CODE	BEST BY DATE
3018CA2CKP	01/18/17
3018CA3CKP	01/18/17
3018CA4CKP	01/18/17
3018CAACKP	01/18/17
3018CABCKP	01/18/17

"The health and safety of our consumers is paramount. As soon as we discovered the issue, we took immediate steps to issue this voluntary recall by alerting our customers who received the product and by asking them to remove it from store shelves," said Shue Wing Chan, President of Tri-Union Seafoods.

No other codes of this product or other Chicken of the Sea products are affected by this voluntary recall.

Consumers looking for additional information can call our 24 hour Recall Information line at 1-800-597-5898.

Contacts

Consumers::

(800)597-5898

Media::

Rebecca Howe Schmidt

Teresa Siles

Nuffer, Smith, Tucker

(619)296-0605

rh@nstpr.com