The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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24751–24775 of 39693

  • SevereNHTSA·16V161000·2016-03-21

    Winnebago Winnie Drop Recalled for Carbon Monoxide Leak Risk

    Winnebago is recalling 2016 Winnie Drop trailers because the refrigerator compartment may not seal properly, allowing carbon monoxide to enter the cabin.

    Product
    WINNEBAGO — WINNEBAGO WINNIE DROP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16125·2016-03-18

    RacerMate Recalls CompuTrainer Blue Flywheels Due to Shattering Risk

    RacerMate is recalling approximately 25,000 CompuTrainer Blue Flywheels because they can shatter during use, posing a risk of injury to riders and bystanders.

    Product
    CompuTrainer Blue Flywheels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V160000·2016-03-18

    GM Recalls 2014-2016 Chevrolet Caprice Police Pursuit for Steering Defect

    General Motors is recalling 2014-2016 Chevrolet Caprice Police Pursuit vehicles because corrosion may cause loss of electric power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CAPRICE POLICE PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V157000·2016-03-17

    Rosenbauer Commander Recall for Brake Pedal Piston Corrosion

    Rosenbauer is recalling 2012-2015 Commander vehicles because brake pedal pistons may corrode, making brakes difficult to activate or causing them to drag.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E021000·2016-03-17

    Battery-Biz Recalls Cyntur Lithium Ion Jumpstarters Due to Fire Risk

    Battery-Biz is recalling Cyntur CTJSLI Lithium Ion Jumpstarters because a faulty cable design may cause overheating and fire. Owners should contact customer service for a free replacement cable.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1063-2016·2016-03-16

    Arrow Percutaneous Insertion Tray Recalled for Potential Sheath Separation

    Arrow International is recalling Percutaneous Insertion Trays because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    Percutaneous Insertion Tray; Product Code: IAK-S7IT The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1058-2016·2016-03-16

    Arrow Ultra 8 IAB Recalled for Potential Sheath Separation and Bleeding Risk

    Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0725-2016·2016-03-16

    Illes Food Ingredients Recalls Asiago Cheese Sauce Seasoning for Salmonella

    Illes Food Ingredients Ltd. is recalling 50 bags of Asiago Cheese Sauce Seasoning because the product tested positive for Salmonella.

    Product
    Asiago Cheese Sauce Seasoning NET CONTENTS: 44.3 POUNDS 20.1 KILOGRAMS packed in flexible bags
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0740-2016·2016-03-16

    R&D Technical Center Recalls Peanut Drop Coating for Listeria

    R&D Technical Center is recalling Clasen Quality Coatings NH Atlas 1M Creamy Peanut Drop after a positive Listeria monocytogenes test.

    Product
    Clasen Quality Coatings NH Atlas 1M Creamy Peanut Drop, Item # 12649, Net Wt. 50 lbs (22.68 KG)
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-1059-2016·2016-03-16

    Arrow UltraFlex IAB Recall: Sheath Separation Risk

    Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    UltraFlex IAB: 7.5Fr 30cc; Product Code: IAB-06830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0733-2016·2016-03-16

    Living Tree Community Foods Recalls Organic Macadamia Nuts Due to Salmonella Risk

    Living Tree Community Foods is recalling 4 oz. pouches of Organic Macadamia Nuts due to potential Salmonella contamination. The recall affects 195 units distributed in 23 US states.

    Product
    Living Tree Community Foods Organic Macadamia Nuts, 4 oz. plastic pouch. Certified Organic
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Devices)·Z-1061-2016·2016-03-16

    Arrow RediGuard IAB Recall Due to Sheath Separation Risk

    Arrow International is recalling RediGuard IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0730-2016·2016-03-16

    Picnic Gourmet Herbed Goat Cheese Spread Recalled for Listeria

    Picnic Gourmet Spreads LLC is recalling Herbed Goat Cheese Spread after a related product tested positive for Listeria monocytogenes.

    Product
    Picnic Gourmet Spreads ( Herbed Goat Cheese Spread) 8 oz containers .12 Containers per case
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0771-2016·2016-03-16

    Tf Supplements Recalls Rhino 7 3000 Due to Undeclared Ingredients

    Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.

    Product
    RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0772-2016·2016-03-16

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.

    Product
    Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0344-2016·2016-03-16

    Homestat Farm Organic Oats Recalled for Salmonella Typhimurium Contamination

    Homestat Farm is recalling Organic Quick Steel Cut Oats & Chia with Flax and Rye Flakes because the flax meal ingredient tested positive for Salmonella Typhimurium.

    Product
    ORGANIC HOMESTAT FARM Quick STEEL CUT OATS & CHIA with Flax and Rye Flakes NET WT 42 OZ (2 LB. 10 OZ.) INGREDIENTS:***organic milled flaxseed*** Distributed by Homestat Farm LTD 6065 Frantz Rd. Suite 206, Dublin, OH 43017 UPC 8 35882 00620 4
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-0734-2016·2016-03-16

    Living Tree Community Foods Recalls Organic Macadamia Butter for Salmonella Risk

    Living Tree Community Foods is recalling Organic Macadamia Butter due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Living Tree Community Foods Organic Macadamia Butter, 8 oz. glass jar. Certified Organic. UPC 64143200987
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Devices)·Z-1057-2016·2016-03-16

    Arrow FiberOptix Ultra 8 IAB recalled for potential sheath separation

    Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, posing a risk of bleeding.

    Product
    FiberOptix Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-LWS The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0726-2016·2016-03-16

    Giant Eagle Recalls Japanese Breaded Cod Fillets Due to Undeclared Soy Allergen

    Giant Eagle is voluntarily recalling Japanese Breaded Cod Fillets sold in Pennsylvania and Ohio because they contain an undeclared soy allergen.

    Product
    Refrigerated, fresh, Panko breaded cod fillet packed in blue foam tray with plastic overwrap. Label reading: Giant Eagle Japanese Breaded Cod Fillet various weights. Distributed by: Giant Eagle, Inc., Pittsburgh, PA 15238 Sold from August 2015 to present with various…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0749-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.

    Product
    Hydromorphone HCL 20 mg/ml/Bupivacaine HCL 40 mg/ml, vol. 20 ml syringe Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0760-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.

    Product
    Hydromorphone HCL 7 mg/ml/Bupivacaine HCL 11.2 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0742-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Sufentanil and Baclofen Syringes

    Hartley Medical Center Pharmacy is recalling Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml syringes due to a lack of assurance of sterility.

    Product
    Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0745-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine Sulfate and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine syringes due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 50 mg/ml/Bupivacaine HCL 24 mg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide