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 deaths or serious injuries are reported, 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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8476–8500 of 113902

  • HighNHTSA·25V376000·2025-07-07

    Kawasaki Ninja ZX-6R Motorcycles Engine Crankshaft Bushing Recall

    Kawasaki is recalling certain 2024–2025 Ninja ZX-6R motorcycles because the engine may lose power during operation due to crankshaft bushing seizure, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-6R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25368·2025-07-03

    Jeriflyer 8-inch Pool Drain Covers Recalled for Entrapment Hazard

    Jeriflyer 8-inch pool drain covers sold on Amazon do not meet federal safety standards and pose a risk of serious injury or death from entrapment. Consumers should immediately stop using affected pools and contact the seller for a refund.

    Product
    Jeriflyer 8-inch pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25372·2025-07-03

    SNLN Party Supply Toys Recalled for Battery Ingestion Hazard

    SNLN Party Supply Toys containing button cell batteries are being recalled because the battery compartments can be easily opened by children, posing a risk of serious injury or death if swallowed.

    Product
    SNLN Party Supply Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25374·2025-07-03

    509 Helmets Recalled Due to Risk of Head Injury

    509 helmets and 509 for Polaris helmets may fail to provide sufficient protection in a crash. One incident reported a helmet detachment during a crash resulting in a concussion.

    Product
    509 helmets and 509 for Polaris helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25367·2025-07-03

    DEWALT Grinder Flap Discs Recalled for Laceration Hazards

    DEWALT has recalled approximately 17,680 Elite Series 40G T27 High Density Flap Discs because the ceramic cloth abrasive flaps can detach during use, causing laceration and injury. Three reports of the flaps detaching resulted in cuts and scrapes.

    Product
    DEWALT® Grinder Flap Discs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25369·2025-07-03

    Trane and American Standard Gas-Electric Packaged Units Recalled for Gas Leak Risk

    Trane U.S. Inc. recalls about 4,790 Gas/Electric Packaged Units because the fuel gas valve can open unexpectedly, causing a gas leak and fire hazard. No injuries have been reported.

    Product
    Trane and American Standard Gas/Electric Packaged Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25371·2025-07-03

    Hyper Tough, Worx, and Portland Electric Chainsaws and Pole Saws Recall

    Positec is recalling about 49,000 Hyper Tough, Worx, and Portland brand electric corded chainsaws and pole saws due to a defective main switch that can fail and allow the saws to continue running, posing a laceration hazard.

    Product
    Hyper Tough, Worx and Portland Chainsaws and Pole Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25366·2025-07-03

    Predator 2000-Watt Power Stations Recalled for Electrical Shock Hazard

    Harbor Freight Tools is recalling about 6,500 Predator 2000-Watt Power Stations due to reversed wires in the AC outlet receptacles when in Emergency Power Supply mode, creating a shock hazard to consumers.

    Product
    Predator 2000W Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V449000·2025-07-03

    Autocar Xspotter and Xpeditor brake air tank recall

    Autocar is recalling certain 2015-2022 Xspotter and Xpeditor vehicles with insufficient air in their brake system tanks. The defect can reduce brake function and increase stopping distance.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·025-2025·2025-07-02

    Kraft Heinz Recalls Oscar Mayer Turkey Bacon Due to Listeria Risk

    Kraft Heinz is recalling Oscar Mayer Turkey Bacon products nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Kraft Heinz Foods Company — Kraft Heinz Foods Company Recalls Turkey Bacon Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0490-2025·2025-07-02

    Fresenius Sodium Chloride Injection Recall: Lack of Sterility Assurance

    Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection in flexible plastic containers nationwide due to lack of assurance of sterility. The FDA classified this as a Class II recall.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0494-2025·2025-07-02

    Ketorolac Tromethamine Ophthalmic Solution Recalled for Sterility Risk

    Apotex Corp. is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% due to lack of assurance of sterility. The recall affects 87,840 bottles distributed nationwide.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0102-2025·2025-07-02

    Mediterranean Pasta Salad Recalled for Salmonella Contamination

    Isabelle's Kitchen, Inc. is recalling Mediterranean Pasta Salad due to Salmonella contamination. The affected product was distributed in Pennsylvania and Maryland.

    Product
    Isabelle's Kitchen, Inc, Maple Avenue Foods Mediterranean Pasta Salad , 4.5 lb., High density polyethylene container with sealed lid.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0111-2025·2025-07-02

    Hy-Vee Duo Crispy Calif Shrimp recalled for Listeria contamination

    Hy-Vee is recalling Duo Crispy Calif Shrimp 10Pc due to potential contamination with Listeria monocytogenes. Affected cases were distributed to retail locations throughout the Midwest.

    Product
    Duo Crispy Calif Shrimp 10Pc
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2023-2025·2025-07-02

    BD BACTEC MGIT 960 PZA Kit tuberculosis susceptibility testing recall

    Becton Dickinson is recalling BD BACTEC MGIT 960 PZA Kit due to reports of intermittent false resistance results during pyrazinamide susceptibility testing of Mycobacterium tuberculosis. The issue affects units distributed worldwide.

    Product
    BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0531-2025·2025-07-02

    Testosterone Cypionate Injection Recalled Without Approved Application

    Advanced Pharmaceutical Technology, Inc. is recalling TESTO-200 (Testosterone Cypionate Injection USP, 200mg/ml) because it was marketed without an approved NDA or ANDA.

    Product
    TESTO-200, Testosterone Cypionate Inj. USP, 2000mg/10ml (200mg/ml), One 10ml multidose vial per carton, For intramuscular injection only, Rx Only, ADVANCED PHARMACEUTICAL TECHNOLOGY, INC., 132 South Central Avenue, Elmsford, NY 10523. NDC 57377-200-01
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·H-0064-2025·2025-07-02

    Grilled Chicken Greek Style Salad recalled due to Salmonella contamination

    Target Corporation is recalling Grilled Chicken Greek Style Salad with Balsamic Dressing because the cucumber may be contaminated with Salmonella. The recall affects 220 units distributed in Illinois, Indiana, Tennessee, and Virginia.

    Product
    Grilled Chicken Greek Style Salad with Balsamic Dressing. Keep Refrigerated. Distributed by SuperTarget, Mpls, MN 55403. Packaged under the following Labels: 1. Good & Gather, Net Wt. 11.0 oz (0.688lb). UPC 233219000008. 2. Boar's Head, Net Wt. 11.2 oz UPC 23321800000
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0481-2025·2025-07-02

    Semaglutide/Cyanocobalamin Injectable Syringes Recalled for Lack of Sterility Assurance

    Thrive Health Solutions is recalling Semaglutide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected lot was distributed nationwide.

    Product
    Semaglutide/Cyanocobalamin Injectable, 5mg/1mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0484-2025·2025-07-02

    Tirzepatide Injections recalled due to lack of sterility assurance

    Thrive Health Solutions is recalling Tirzepatide Injections 30mg/mL pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Tirzepatide Injections, 30mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1904-2025·2025-07-02

    Broselow Pediatric Emergency Rainbow Tape recalled for incorrect dosing values

    SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to incorrect values printed on the tape that could lead to improper medication dosing and defibrillation in pediatric emergency care.

    Product
    Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0067-2025·2025-07-02

    Salted Smoked Split Herring Recalled for Botulinum Contamination

    P East Trading Corp is recalling Salted Smoked Split Herring due to potential Clostridium botulinum contamination in uneviscerated fish. The product was distributed to retail locations in New York, New Jersey, and Connecticut.

    Product
    Salted Smoked Split Herring, approximately 12 inches in length; packaged in 18 lb wooden box and repacked at retail in deli-style or other retail packaging (for a list of retail locations see associated press release)
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0473-2025·2025-07-02

    Metoclopramide Tablets Recalled for Presence of Foreign Tablets

    Teva Pharmaceuticals USA, Inc. is recalling Metoclopramide Tablets, USP 10 mg due to the presence of foreign tablets or capsules in the product. The affected lot is distributed nationwide.

    Product
    METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0480-2025·2025-07-02

    Semaglutide pre-filled syringe recalled due to sterility concerns

    Thrive Health Solutions is recalling Semaglutide 5 mg/mL pre-filled syringes distributed nationwide because the manufacturer cannot assure the product's sterility.

    Product
    Semaglutide, 5 mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide