Category Archives: Recall

Halo, Purely for Pets® Issues Voluntary Recall of Sensitive Cat Turkey Dry Food Due to Mold

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ucm472417Halo, Purely for Pets has initiated a limited, voluntary recall of its Spot’s Stew Sensitive Cat Turkey kibble with a Best By date of 09/04/2016 due to reports of mold. No other Halo products are affected.

Consumers who have Spot’s Stew Sensitive Cat Turkey stamped “Best By 09/04/2016” should discontinue feeding, and return the remaining portion to any Halo retailer for a full refund or replacement.

While some pets can ingest mold without incident, others may experience digestive issues. Consumers should consult their veterinarian if their cat experiences digestive issues.
Halo is also instructing its retailers to remove Sensitive Cat Turkey products stamped “Best By 09/04/2016” from their shelves.

The affected product is:

Product name:
Spot’s Stew Wholesome Turkey Recipe Sensitive Formula for Cats

UPC Codes:
745158350231 and 745158340232

Sizes:
6 lb. and 3 lb. bags

Best by Date:
09/04/2016

For more information, contact Halo Customer Care at 800-426-4256 Monday-Friday 8:00 a.m. – 5:00 p.m. EST, or email customers@halopets.com or visit www.halopets.comdisclaimer icon.

Blue Buffalo Company, Ltd. Voluntarily Recalls Limited Production of Kitty Yums Chicken Recipe Cat Treats

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catyums-1Blue Buffalo Company, Ltd. is voluntarily recalling a limited production of Blue Kitty Yums Chicken Recipe Cat Treats that may contain low levels of propylene glycol, which is not permitted by the FDA for use in cat food.

Cats reacting to high doses of propylene glycol may exhibit signs of depression and may have a loss of coordination, muscle twitching, and excessive urination and thirst. If your cat has consumed the recalled product and has these symptoms, please contact your veterinarian.

The affected product was distributed nationwide in the US and Canada through pet specialty stores and e-commerce.

The product is packaged in a 2 oz., plastic stand up pouch. Only these specific code dates of this product are involved:

* Blue Kitty Yums Tasty Chicken Recipe, UPC: 859610007820 – Best If Used By: April 24, 2016.
* Blue Kitty Yums Tasty Chicken Recipe, UPC: 859610007820 – Best If Used By: July 24, 2016.

No other BLUE pet foods or treats are involved in this recall.

The FDA tested product in response to a single consumer complaint and found propylene glycol in one bag of our cat treats in the impacted lot. To date we have had no other reports of incidents related to our cat treats. Out of an abundance of caution, we are voluntarily recalling all product manufactured in the same lot as the subject bag.

Consumers who have purchased the product being recalled may return it to the place of purchase for a full refund. Consumers with questions may contact Blue Buffalo at: 888-667-1508 from 8 AM to 5 PM Eastern Time Monday through Friday and the weekend of November 7, 2015 or by email at BlueBuffalo5883@stericycle.com for more information.

David Trail Mix Sweet & Salty Voluntarily Recalled Due To Undeclared Dairy Allergen

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daves-1DAVID® Trail Mix Sweet & Salty flavor is being voluntarily recalled by ConAgra Foods of Omaha, Nebraska, due to the presence of an ingredient in the trail mix that contains milk protein, which is not declared on the packaging.

The finished product is made for ConAgra Foods by a third party supplier who is conducting a separate recall for similar, impacted products.

This food is a concern for people who are allergic to milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume the product. ConAgra Foods was made aware of this issue through a consumer contact. ConAgra Foods is aware of one consumer allergic reaction associated with consumption of this product.

ConAgra Foods is advising consumers who have purchased this item to discard it or return it to the store where originally purchased.

This recall includes the following DAVID Trail Mix Sweet & Salty products sold as part of multi variety packages that also contain DAVID Trail Mix Classic. DAVID Trail Mix Classic is not impacted by this recall.

The DAVID Trail Mix Sweet & Salty UPC is: 26200 23885, 5oz. bags/149g.

The product was shipped to retail food stores and distributors in the U.S. and Mexico. ConAgra Foods is working with retail customers and distributors to ensure the packages are removed from store shelves.

This recall is limited to DAVID Trail Mix Sweet & Salty flavor only and does not impact other flavors of DAVID Trail Mix or any DAVID Seeds products.

Consumers with questions should call our Consumer Affairs hotline at: (800) 881-3989, open 24 hours a day/7 days a week.

General Mills Issues Voluntary Recall Of Cheerios And Honey Nut Cheerios Cereal

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800-cheerios-1MINNEAPOLIS, Minnesota — General Mills is voluntarily recalling several days of production of Cheerios and Honey Nut Cheerios cereal produced at its Lodi, California facility on certain dates in July of this year because of an undeclared allergen – wheat – with potential adverse health effects.

Cheerios and Honey Nut Cheerios produced on these dates at the company’s Lodi, California facility are being recalled because an isolated incident resulted in wheat flour being inadvertently introduced into the gluten free oat flour system at its Lodi facility. As a result, the products may contain an undeclared allergen – wheat – in products labeled as gluten-free.

General Mills will recall and retrieve affected cereals produced on those dates from customer warehouses and store shelves. Consumers with wheat allergies, celiac disease or gluten intolerance should not consume products bearing the affected code dates and should contact General Mills for a replacement or full refund.

This voluntary recall includes four days production of original (yellow box) Cheerios, and thirteen days of production of Honey Nut Cheerios at its Lodi, California facility with the following “BETTER IF USED BY” code dates and the plant code LD which indicates the product was produced at Lodi, California:

Honey Nut Cheerios
12JUL2016LD, 17JUL2016LD, 23JUL2016LD, 13JUL2016LD, 18JUL2016LD, 24JUL2016LD, 14JUL2016LD, 20JUL2016LD, 25JUL2016LD, 15JUL2016LD, 21JUL2016LD, 16JUL2016LD, 22JUL2016LD

Yellow Box Cheerios
14JUL2016LD, 15JUL2016LD, 16JUL2016LD, 17JUL2016LD

Products containing wheat can cause illness or severe reactions for individuals with wheat allergies or celiac disease. Products containing wheat can also cause illness or discomfort for individuals with gluten intolerance.

General Mills is transitioning five varieties of Cheerios to gluten free. Cheerios and Honey Nut Cheerios cereals produced at General Mills’ other facilities, or on dates other than those noted at the Lodi, California facility, are not impacted. General Mills’ other gluten-free Cheerios varieties – including Apple Cinnamon Cheerios, Frosted Cheerios and MultiGrain Cheerios – are not impacted and are not being recalled. No other General Mills cereals are affected

Consumers requesting refunds or calling with further questions should contact General Mills Consumer Services at 1-800-775-8370.

K-9 Kraving Dog Food Has Announced a Voluntary Recall of Their Chicken Patties Dog Food

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k9-cravingBaltimore, MD — K-9 Kraving Dog Food has announced a voluntary recall of their Chicken Patties Dog Food shipped between July 13th – July 17th, 2015 because these products may be contaminated with Salmonella and Listeria monocytogenes. Salmonella and Listeria monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

Healthy people infected with Salmonella and Listeria monocytogenes should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella and Listeria monocytogenes 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.

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

The affected product was distributed to retail stores only in Maryland. No other K-9 Kraving Dog Food products are affected.

No illnesses have been reported to date. Even though no illnesses have been reported, consumers should follow the Safe Handling Instructions printed on the K-9 Kraving Dog Food package when disposing of the affected product.

K-9 Kraving Dog Food became aware of a potential issue after receiving notification from the FDA that a routine surveillance sample of Chicken Patties tested positive for Salmonella and Listeria monocytogenes.

Consumers feeding the affected product should discontinue use and monitor their pet’s health, and contact their veterinarian if they have concerns. Consumers who purchased the product can obtain a full refund or exchange by either returning the product in its original packaging or bringing a proof of purchase back to their retailer.

Consumers with additional questions can call our Consumer Relations team at 1-800-675-1471 from 8:00 a.m. to 3:00 p.m., Monday through Friday, EST.

Robert Barrett, Chief Executive Officer of K-9 Kraving Dog Food, stated, “At K-9 Kraving Dog Food we take quality and safety very seriously. We believe that under all circumstances, health and safety comes first, and we are committed to providing the best possible nutrition for pets.”

One lot of “Good ‘N’ Fun – Beefhide Chicken Sticks” recalled due to possible salmonella contamination

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GoodnFun-1Deerfield, FLORIDA — Salix Animal Health, LLC today announced it has initiated a voluntary recall of one lot of “Good ‘n’ Fun – Beefhide Chicken Sticks” because it may have the potential to be contaminated with Salmonella. Salmonella can affect animals eating the product and there is risk to humans from handling contaminated products.

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.

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

The recalled “Good ‘n’ Fun – Beefhide Chicken Sticks” was distributed nationwide by Salix Animal Health to Dollar General and Dollar Tree retail stores.

The recalled product is packaged in a 2.8 ounce bag stamped on the back side with lot # AO15010 and with an expiration date of 03/2018. The UPC code is 0 91093 82247 1.

No pet or consumer illnesses from this product have been reported to date. However, because of our commitment to safety and quality, Salix Animal Health is conducting a voluntary recall of this product.

The potential for contamination was noted after routine testing by the Georgia Department of Agriculture revealed the presence of Salmonella in one 2.8 ounce package of “Good ‘n’ Fun – Beefhide Chicken Sticks” labeled with the recalled code.

No other product is affected at this time. Customers should look at the lot code and expiration date on the product package to determine if it is subject to the voluntary recall. Customers who have purchased the product subject to this recall are urged to dispose of the product or return it for full refund.

We take our responsibility to pets and their owners seriously and as a result we are investigating the cause of this problem so that we can prevent it from occurring in the future. Salix Animal Health, is also working with retailers to ensure that the affected product is no longer sold and removed from inventory.

If you have these products, please contact Salix Animal Health’s consumer affairs team at 1-800-338-4896, Monday through Friday between the hours of 8:30 AM – 5:00 PM Eastern Standard Time for a refund. Customers with questions may call the consumer affairs team at the number listed above.

OC RAW DOG Voluntarily Recalls Limited Number of Raw Frozen Dog Food Due to Potential Salmonella Health Risk

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Santa Margarita, CALIFORNIA — OC Raw Dog of Rancho Santa Margarita, CA is voluntarily recalling 640 lbs. of Chicken, Fish & Produce Raw Frozen Canine Formulation. This is being done in an abundance of caution, as the product has the potential to be contaminated with Salmonella. No illnesses have been reported and no other OC Raw Dog manufactured products are affected.

Individuals handling raw pet food can become infected with salmonella, especially if they have not thoroughly washed their hands after having contact with the product or to surfaces exposed to the product. 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. If a consumer exhibits these signs after having contact with this product should contact their healthcare providers.

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

This voluntary recall is limited to Chicken, Fish & Produce Raw Frozen Canine Formulations that were packaged into 6.5 lb. Doggie Dozen Patties, 4 lb. Doggie Sliders, and 3 lb. Meaty Rox with the lot number 1819, and use by date of 05/05/16. These codes can be checked on the bottom left corner of the back of the package. Distribution is limited to customers in Colorado, Vermont, and Pennsylvania and sold to consumers through independent pet specialty retailers.

The potential for contamination was noted after routine testing by the Colorado Department of Food and Agriculture of a sample that they collected at retailer revealed the presence of Salmonella in a 3 lb. bag of “Chicken, Fish & Produce Raw Frozen Canine Formulations” Meaty Rox. Another sample from the same lot was previously tested by the California Department of Agriculture and it had a negative Salmonella result.

If you are in possession of this recalled product please submit a picture of the package with the lot number to Olivia@ocrawdog.com for verification. Either dispose of the product immediately or return the product to the retailer where you purchased it for a replacement product.

Consumers with questions may contact the company at 1-844-215-DOGS (3647) Monday thru Friday 9am – 4pm PST. If you get our automated answering system please leave a message and we will call you right back.

At OC RAW DOG, we are passionate about our products and the safety of canine and human customers is our top priority. We apologize for any inconvenience this recall may have caused.
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OC-RAW-2
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Kraft Heinz Foods Company Recalls Turkey Bacon Products Due To Possible Adulteration

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Kraft-2WASHINGTON — Kraft Heinz Foods Company, a Newberry, S.C. establishment, is recalling approximately 2,068,467 pounds of turkey bacon products that may be adulterated because it may spoil before the “Best When Used By” date, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The problem was discovered by the establishment during an investigation into spoilage-related consumer complaints. The turkey bacon was produced between May 31, 2015, and August 6, 2015. The following products are subject to recall:

  1. 56 oz. cardboard boxes (containing four plastic wrapped packages) marked Oscar Mayer “Selects Uncured Turkey Bacon” bearing the plant number P-9070, the line number RS19 and Product UPC 0 4470007633 0, and with “Best When Used By” dates of 24 AUG 2015 through 26 OCT 2015.
  2. 36 oz. cardboard boxes (containing three plastic wrapped packages) marked Oscar Mayer Turkey Bacon “Smoked Cured Turkey Chopped and Formed” bearing the plant number P-9070, the line number RS19 and Product UPC 0 7187154874 8, and with “Best When Used By” dates of 28 AUG 2015 through 20 OCT 2015.
  3. 48 oz. cardboard boxes (containing four plastic wrapped packages) marked Oscar Mayer Turkey Bacon “Smoked Cured Turkey Chopped and Formed” bearing the plant number P-9070, the line number RS19 and Product UPC 0 7187154879 3, and with “Best When Used By” dates of 3 SEPT 2015 through 30 OCT 2015.

The products subject to recall bear the establishment number “P-9070” inside the USDA mark of inspection, as well as the line number “RS19”. These items were shipped nationwide and exported to the Bahamas and St. Martin.

FSIS has not received any confirmed reports of adverse reactions related to the consumption of these products. However, the company has received reports of illness related to the consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products

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On July 2, 2015, Cook Medical initiated a lot-specific voluntary recall of 2,239 lots of Beacon Tip Angiographic Catheters. Globally, 95,167 devices are subject to this recall. The products include specific versions and lot numbers of the Torcon NB® Advantage Beacon® Tip Catheters (Catalog Prefix HNBR5.0), Royal Flush® Plus Beacon® Tip High-Flow Catheters (Catalog Prefix HNR4.0), and Slip-Cath® Beacon® Tip Catheters (Catalog Prefix SCBR5.0).

The Beacon Tip Angiographic Catheters have been found to exhibit tip splitting or separation, which has resulted in adverse events. Cook has received 26 complaints of catheter-tip splitting and/or separation. There have been 14 Medical Device Reports to date in which a tip split or separation occurred.

Tip splitting has the potential to lead to loss of device function. Tip separation may require medical intervention to retrieve a separated segment or may occlude blood flow to end organs.

The Beacon Tip Angiographic Catheters in this recall were distributed between June 2013 and June 2015. Product can be identified by the part number and lot number provided on the outer package product label. The lot numbers for products that are subject to this recall can be found on the following pages.

Cook Medical has notified its customers and distributors by recall notification letters. The letters requested that all customers and distributors quarantine and discontinue use of all potentially affected units and return the affected product to the company as soon as possible for credit.

FDA and other regulatory agencies around the world have been notified of this action.

The full list of recalled products can be found at the FDA web site.

U.S. DOT announces Fiat Chrysler enforcement action.

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WASHINGTON – U.S. Transportation Secretary Anthony Foxx announced today that Fiat Chrysler Automobiles has acknowledged violations of the Motor Vehicle Safety Act’s requirements to repair vehicles with safety defects and will submit to rigorous federal oversight, buy back some defective vehicles from owners, and agreed to a $105 million civil penalty, the largest ever imposed by the Department’s National Highway Traffic Safety Administration.

Chrysler FAQ (PDF)

The enforcement action comes after a July 2 public hearing at which NHTSA officials outlined problems with Fiat Chrysler’s execution of 23 vehicle safety recalls covering more than 11 million defective vehicles. Fiat Chrysler has since admitted to violating the Safety Act in three areas: effective and timely recall remedies, notification to vehicle owners and dealers and notifications to NHTSA.

This recall effects 1,771 2014-2015 model years Ram 4500 and 5500 manufactured August 20, 2013, to January 27, 2015, and equipped with 6.4L Hemi engines. Chrysler has also recalled 644,354 2011-2014 model years Jeep Grand Cherokee vehicles manufactured from January 5, 2010, through September 8, 2013 and 2011-2014 model years Dodge Durango vehicles manufactured from January 5, 2010, through September 8, 2013

“Today’s action holds Fiat Chrysler accountable for its past failures, pushes them to get unsafe vehicles repaired or off the roads and takes concrete steps to keep Americans safer going forward,” said Secretary Foxx. “This civil penalty puts manufacturers on notice that the Department will act when they do not take their obligations to repair safety defects seriously.”

In a consent order issued by NHTSA, Fiat Chrysler commits to take action to get defective vehicles off the roads or repaired. Owners of more than half a million vehicles with defective suspension parts that could cause the vehicle to lose control will have the opportunity to sell their vehicle back to Fiat Chrysler. Owners of more than a million Jeeps that are prone to deadly fires either will have the chance to trade their vehicle in for above its market value, or will receive a financial incentive to get their vehicle remedied.

The consent order requires FCA to notify vehicle owners eligible for buybacks and other financial incentives that these new options are available.

The automaker also agrees to unprecedented oversight for the next three years, which includes hiring an independent monitor approved by NHTSA to assess, track and report the company’s recall performance.

“Fiat Chrysler’s pattern of poor performance put millions of its customers, and the driving public, at risk,” NHTSA Administrator Mark Rosekind said. “This action will provide relief to owners of defective vehicles, will help improve recall performance throughout the auto industry, and gives Fiat Chrysler the opportunity to embrace a proactive safety culture.”

The company must pay a $70 million cash penalty – equal to the record $70 million civil penalty the agency imposed on Honda in January. In addition, Fiat Chrysler must spend at least $20 million on meeting performance requirements included in the Consent Order. Another $15 million could come due if the independent monitor discovers additional violations of the Safety Act or the Consent Order.