Real-time live feed from the FDA for any recalls of cat food or other cat related products, as well as any Animal & Veterinary news from the FDA.

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Recalls of cat food or other cat related products
Animal & Veterinary news from the FDA

 

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What’s New: Animal & Veterinary


  • Wed, 17 Jan 2018 03:16:00 -0700: Federal Register Notices - What's New: Animal & Veterinary
    Federal Register notices issued by the Center for Veterinary Medicine.
  • Tue, 09 Jan 2018 07:36:00 -0700: Recent Animal Drug Approvals - What's New: Animal & Veterinary
    Animal drug approval information including name, species and indications for use from the last six months.
  • Tue, 09 Jan 2018 06:30:00 -0700: Medicated Feeds - What's New: Animal & Veterinary
    An approved medicated feed mill license is required for facilities that manufacture feed using certain medicated articles/drugs.
  • Tue, 09 Jan 2018 03:36:00 -0700: Veterinary Feed Directive (VFD) - What's New: Animal & Veterinary
    A VFD drug is intended for use in animal feeds, and such use of the VFD drug is permitted only under the professional supervision of a licensed veterinarian.
  • Thu, 04 Jan 2018 08:40:00 -0700: Food Safety Modernization Act and Animal Feed - What's New: Animal & Veterinary
    This page highlights FSMA content that will be of most interest to manufacturers and distributors of animal food.
  • Wed, 20 Dec 2017 15:04:00 -0700: FDA Clarifies Approved Free-Choice Feeding Options for Anaplasmosis Control in Cattle - What's New: Animal & Veterinary
    FDA provided Question and Answers to assist with the appropriate selection and use of approved VFD free-choice medicated feed products for the control of active infection of anaplasmosis in cattle.

 

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Recalls of cat food or other cat related products
Animal & Veterinary news from the FDA

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  • Thu, 18 Jan 2018 08:53:00 -0700: Allergy Alert Issued in Select North Atlantic Whole Foods Market Stores for Undeclared Almond Flour in Cheesecake Bars - Food and Drug Administration--Recalls/Safety Alerts
    CAMBRIDGE, Massachusetts (January 15, 2018) – Nine Whole Foods Market stores in Connecticut, Massachusetts, and Rhode Island are voluntarily recalling cheesecake bars because the product potentially contained a tree nut allergen (almond flour) that was not listed on the product label. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reactions if they consume these products
  • Wed, 17 Jan 2018 20:27:00 -0700: Palmer Candy Company Announces Voluntary Recall of Sea Salt Caramel Hearts - Food and Drug Administration--Recalls/Safety Alerts
    Palmer Candy Company (www.palmercandy.com), announced today a limited recall of Sea Salt Caramel Hearts that were only sold at Bomgaards Supply Inc. Store in the Midwest States. The voluntary recall, in cooperation with the U.S. Food and Drug Administration (FDA) due to abundance of caution of a possible peanut allergen contamination. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
  • Wed, 17 Jan 2018 16:49:00 -0700: AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Levofloxacin in 5% Dextrose 250mg/50mL Due to Presence of Visible Particulate Matter Tentatively Identified as Mold - Food and Drug Administration--Recalls/Safety Alerts
    FOR IMMEDIATE RELEASE – 01-12-2018 – East Windsor, New Jersey, AuroMedics Pharma LLC is voluntarily recalling one lot of Levofloxacin in 5% Dextrose Injection 250mg/50mL in a Single-Use flexible container NDC 55150-243-46, Lot CLF160003, Expiry date May 2018, to the hospital level. The product has been found to contain visible particulate matter tentatively identified as mold. This problem was discovered as a result of a product complaint in which the contents of one flexible bag was found to contain white particulate matter
  • Tue, 16 Jan 2018 19:02:00 -0700: Baxter Expands Voluntary Nationwide Recall to Include Second Lot of Nexterone Injection Due to Presence of Particulate Matter - Food and Drug Administration--Recalls/Safety Alerts
    Following the issuance of a voluntary recall dated November 10, 2017 of one lot of NEXTERONE (amiodarone HCl) 150 mg/100 mL Premixed Injection, Baxter International Inc. announced today it is expanding the recall to include a second lot (NC109123) of NEXTERONE due to the potential presence of particulate matter.
  • Tue, 16 Jan 2018 14:31:00 -0700: Bellisio Foods, Inc. Issues Allergy Alert Regarding Certain Michelina’s Fettuccine Alfredo Packages Due to Potential Presence of Undeclared Soy - Food and Drug Administration--Recalls/Safety Alerts
    Bellisio Foods, Inc., a Jackson, Ohio, manufacturer, is voluntarily recalling certain Michelina’s Fettuccine Alfredo due to the possibility some packages may contain undeclared chicken with soy that is not listed on packaging. People who have an allergy or sensitivity to soy may run the risk of serious allergic reaction(s) if they consume this product.
  • Sat, 13 Jan 2018 13:31:00 -0700: Hiland Dairy Announces Voluntary Recall Of Hiland Dairy Orange Juice And Tampico Citrus Punch - Food and Drug Administration--Recalls/Safety Alerts
    Hiland Dairy is announcing a voluntary recall of two products produced at the Omaha, Nebraska facility, over concerns the products may contain milk protein that could affect those individuals that have sensitivity to milk allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. No illnesses or allergic reactions have been reported at this time.
  • Fri, 12 Jan 2018 13:41:00 -0700: Rico Brand Issues Allergy Alert on Undeclared Soy in Tofu Breakfast Burrito - Food and Drug Administration--Recalls/Safety Alerts
    Rico Brand of Salt Lake City, Utah is recalling Tofu Breakfast Burrito, because it may contain undeclared Soy. People who have an allergy or severe sensitivity to Soy run the risk of serious or life-threatening allergic reaction if they consume these products.
  • Thu, 11 Jan 2018 22:45:00 -0700: Fieldbrook Foods Corporation Clarifies Scope of its Voluntary Recall. Products Include Orange Cream - Food and Drug Administration--Recalls/Safety Alerts
    Fieldbrook Foods Corporation is clarifying that the previously announced voluntary recall of all orange cream bars and chocolate coated vanilla ice cream bars that were produced in 2017 on the company’s Hoyer 1 Line at its Dunkirk, NY plant (plant code 362677) also includes 28,751 cases of Raspberry Cream Bars that were included with Orange Cream Bars in ALDI seasonal split-case purchases.
  • Thu, 11 Jan 2018 18:06:00 -0700: Hom/Ade Foods, Inc. Voluntarily Recalls Frozen Biscuits Because of Possible Health Risk - Food and Drug Administration--Recalls/Safety Alerts
    Hom/Ade Foods, Inc is voluntarily recalling Mary B’s® brand biscuits due to potential contamination with Listeria monocytogenes. The problem was discovered in a product sampling conducted by an outside co-packer, who manufactured the product.
  • Thu, 11 Jan 2018 13:55:00 -0700: Pharmedium Services, LLC Expands Voluntary Nationwide Recall of Additional Lots of Compounded Sterile Products Within Expiry Due to Lack of Sterility Assurance - Food and Drug Administration--Recalls/Safety Alerts
    January 10, 2018 Lake Forest, IL PharMEDium Services, LLC (PharMEDium) is voluntarily expanding the recall issued on December 27, 2017 to include the below lots of sterile drug products to the hospital/user level due to a lack of assurance of sterility. Administration of a drug product intended to be sterile that is not sterile could result in serious infections that may be life-threatening.
  • Thu, 11 Jan 2018 12:52:00 -0700: Gilster - Mary Lee Corp. Issues a Recall For Undeclared Milk Allergen in Essential Everyday® Chicken Coating - Food and Drug Administration--Recalls/Safety Alerts
    January 8, 2018 - Gilster-Mary Lee, 520 Old St. Mary’s Road, of Perryville, Missouri, is voluntarily recalling one lot of Essential Everyday® Coat & Bake Original Chicken coating, UPC 41303-01572 at the consumer level because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
  • Wed, 10 Jan 2018 09:54:00 -0700: International Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel Tablets USP, 75 mg packaged in bottles of 30 tablets Due to Mislabeling NDC # 54458-888-16; Lot # 117099A - Food and Drug Administration--Recalls/Safety Alerts
    International Laboratories, LLC is voluntarily recalling Lot# 117099A of Clopidogrel Tablets, USP 75 mg, packaged in bottles of 30 tablets, to the consumer level due to mislabeling. The product is labeled as Clopidogrel tablets USP 75 mg but may contain Clopidogrel 75mg or Simvastatin Tablets USP 10 mg.
  • Wed, 10 Jan 2018 07:59:00 -0700: Wells Collection Inc Issues Alert On Undeclared Sulfites In Rely Brand Dried Longya Lily - Food and Drug Administration--Recalls/Safety Alerts
    Wells Collection Inc of Brooklyn, NY, is recalling its 8 ounce packages of Rely Brand Dried Longya Lily because the product contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
  • Tue, 09 Jan 2018 20:38:00 -0700: Fieldbrook Foods Corporation, Announces an Extension of Voluntary Recall of Orange Cream Bars and Chocolate Coated Vanilla Ice Cream Bars for Possible Health Risk - Food and Drug Administration--Recalls/Safety Alerts
    Fieldbrook Foods Corporation has issued a voluntary recall of all orange cream bars and chocolate coated vanilla ice cream bars that were produced in 2017 on the company’s Hoyer 1 Line at its Dunkirk, NY plant (plant code 362677). This is the only production line and the only Fieldbrook Foods plant (of 3) involved in this recall notice. Both products are being recalled due to the possibility that they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short- term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  • Tue, 09 Jan 2018 17:03:00 -0700: Dollar General Announces Voluntary Recall of Clover Valley® Iced Oatmeal Cookies Over Undeclared Milk and Tree Nuts - Food and Drug Administration--Recalls/Safety Alerts
    Dollar General Corporation announced a voluntary recall of its 12-ounce packages of Clover Valley® Iced Oatmeal Cookies with lot # L46217 30 with a best-by date of August 18, 2018 over concerns of undeclared milk and tree nuts. Consumers with a milk and/or nut allergy or sensitivity to these items should not consume these products due to a possible health risk or serious allergic reaction. No illnesses or reactions have been reported at this time.
  • Fri, 05 Jan 2018 16:58:00 -0700: Fieldbrook Foods Corporation, Announces a Voluntary Recall of Orange Cream Bars for Possible Health Risk - Food and Drug Administration--Recalls/Safety Alerts
    Fieldbrook Foods Corporation of Dunkirk NY has issued a voluntary recall of 20 cases of the Tops brand of Orange Cream Bars and 320 cases of the Meijer Purple Cow brand Orange Cream Bars due to the possibility that the product may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
  • Fri, 05 Jan 2018 14:54:00 -0700: Hong Lee Trading Inc. Issues Allergen Alert on Undeclared Milk Allergens in Chao Café Vietnamese Instant Coffee Mixed 3 in 1 - Food and Drug Administration--Recalls/Safety Alerts
    Hong Lee Trading Inc., NY, is recalling its CHAO CAFÉ VIETNAMESE INSTANT COFFEE MIXED 3 IN 1, 384 GRAM, CONTAINER CODE JUNE 06 2018, because they contain undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life-threatening allergic reactions if they consume this product.
  • Thu, 04 Jan 2018 08:02:00 -0700: Condies Foods Issues Allergy Alert on Undeclared Milk and Egg allergen in Veggie Cup Item# 40781 - Food and Drug Administration--Recalls/Safety Alerts
    Condies Foods of Kearns, UT is recalling 166 cases of code date “USE THRU 01/05/2018,” there is a possibility that this may contain undeclared milk and egg allergens. People who have an allergy or severe sensitivity to milk and egg run the risk of serious or life-threatening allergic reaction if they consume these products.
  • Thu, 04 Jan 2018 07:36:00 -0700: Evershing International Trading Company Recalls Frozen Shredded Coconut Because of Possible Health Risk - Food and Drug Administration--Recalls/Safety Alerts
    Evershing International Trading Company is recalling 16 ounces Coconut Tree Brand Frozen Shredded Coconut because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune system. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting in to the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. No illnesses have been reported to date.
  • Wed, 03 Jan 2018 15:05:00 -0700: Auromedics Pharma LLC Issues Voluntary Nationwide Recall of Product Ampicillin and Sulbactam for Injection USP 1.5 g/ Vial, Due to Presence of Glass Particles in the Vial - Food and Drug Administration--Recalls/Safety Alerts
    AuroMedics Pharma LLC is voluntarily recalling lot AFO l 17001-A, Expiry date Dec 2018, of Ampicillin and Sulbactam for Injection USP, 1.5 g (equivalent to 1 g ampicillin as the sodium salt plus 0.5 g Sulbactam as the sodium salt) in a Single-Dose vial, to the hospital level. The product has been found to contain glass particles.

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