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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22976–23000 of 26060

  • HighFDA (Devices)·Z-0516-2022·2022-02-02

    Artis icono diagnostic imaging system software defects recalled nationwide

    Siemens is recalling 72 units of Artis icono biplane diagnostic imaging systems nationwide due to four software issues that could disable x-ray capability, corrupt diagnostic images, or cause unexpected shutdowns during procedures.

    Product
    Artis icono biplane with software VE20C-diagnostic imaging angiography system Model: 11327600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0619-2022·2022-02-02

    Frozen Tuna Steaks Recalled for Elevated Histamine Levels

    Relish Foods, Inc. dba Gourmet Fusion Foods is recalling 10 oz. individually wrapped frozen tuna steaks due to elevated histamine levels detected in FDA consumer samples.

    Product
    10 oz. individually wrapped frozen tuna steaks; 4 servings per bag Important: Thaw under refrigeration immediately before use. May contain bones. Product must be cooked prior to consumption KEEP FROZEN AT -18 CELSIUS OR BELOW THAW UNDER REFRIGERATION IMMEDIATELY BEFORE
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0526-2022·2022-02-02

    Footrest accessory recalled for missing friction rubber block

    FDA recalls Intelli-C footrest accessories due to missing friction rubber blocks in the clamping mechanism. The defect may cause the footrest to slip during use.

    Product
    1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Drugs)·D-0423-2022·2022-02-02

    Betadine Sterile Ophthalmic Solution Recalled for Sterility Assurance

    Edge Pharma is recalling Betadine sterile ophthalmic solution syringes due to lack of assurance of sterility. The affected product is a preservative-free, single-use ophthalmic solution distributed nationwide.

    Product
    Betadine (povidone-iodine), Sterile Ophthalmic Solution, Preservative Free, 5% 0.5mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446, NDC 05446-1680-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0528-2022·2022-02-02

    MAGEC 1 System Recalled for Post-Implantation Component Fractures

    The MAGEC 1 System implantable medical device is being recalled due to documented post-implantation fractures of an internal metallic component. The recall affects approximately 3,056 units manufactured before March 26, 2015 and distributed worldwide.

    Product
    MAGEC 1 System
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·22069·2022-02-02

    SureClose READYFIT 180° Hinge-Closer Sets Recalled for Drowning Hazard

    D&D Technologies is recalling about 1,500 SureClose READYFIT 180° hinge-closer sets because they can malfunction and fail to fully self-close gates, allowing unintended access to pools and posing injury and drowning hazards to young children.

    Product
    SureClose® READYFIT 180° Hinge-Closer Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0517-2022·2022-02-02

    Diagnostic Imaging Angiography System Software Defects Recalled by Siemens

    Siemens is recalling 23 Artis icono angiography systems due to four software defects that could disable imaging, corrupt images, and cause unexpected shutdowns during patient procedures.

    Product
    Artis icono floor with software VE20C-diagnostic imaging angiography system Model: 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0617-2022·2022-02-02

    G&C Foods Gouda Cheese Recall for Undeclared Wheat

    G&C Food Distributors & Brokers Inc. is recalling Gouda cheese that may contain undeclared wheat. The product was distributed to food service facilities in Connecticut, New Jersey, New York, Pennsylvania, and Tennessee.

    Product
    GOUDA CHEESE; INGREDIENTS: CULTURED PASTEURIZED MILK, SALT, ENZYMES, ANNATTO COLOR; Distributed By: G&C Foods; ALLERGEN: MILK; CONTAINS: 1 BAG; Product is for Food Service Only; KEEP REFRIGERATED
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-0417-2022·2022-02-02

    Phenylephrine HCl Injection Recalled Due to Lack of Sterility Assurance

    Edge Pharma is recalling approximately 5,335 syringes of Phenylephrine HCl Sterile Solution for Injection nationwide due to lack of assurance of sterility. The product may not meet sterility requirements for safe use.

    Product
    Phenylephrine HCl, Sterile Solution for Injection, (PF), 800 mcg/10mL (80 mcg/mL), Single Use Syringe for IV Injection, Edge Pharma, LLC 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1652-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0620-2022·2022-02-02

    Bake Crafters Maple Waffle Chicken Sausage Recalled for Listeria Contamination Risk

    Bake Crafters is recalling Maple Waffle WG Chicken Sausage due to potential Listeria monocytogenes contamination. The affected products were distributed to distribution centers in Idaho and Pennsylvania.

    Product
    Bake Crafters - Maple Waffle WG Chicken Sausage Packaged into cardboard containers 126 units per case
    Category
    Food
    Distribution
    2 states
  • HighCPSC·22068·2022-02-02

    Maxtrade Youth ATVs Recalled for Speed and Brake Safety Defects

    About 141,000 Maxtrade Coolster Mountopz youth all-terrain vehicles fail to meet federal safety standards. The ATVs exceed maximum speed limits for their intended age groups and some have parking brakes that do not prevent vehicle movement, posing a risk of serious injury or death.

    Product
    Maxtrade's Youth Coolster Mountopz All-Terrain Vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0616-2022·2022-02-02

    White Cheddar Cheese Recalled for Undeclared Wheat

    G&C Food Distributors & Brokers Inc. is recalling white cheddar cheese distributed to Connecticut, New Jersey, New York, Pennsylvania, and Tennessee because the product may contain undeclared wheat, which poses a risk to consumers with wheat allergies.

    Product
    WHITE CHEDDAR CHEESE; INGREDIENTS: CULTURED PASTEURIZED MILK, SALT, ENZYMES; Distributed By: G&C Foods; ALLERGEN: MILK; CONTAINS: 1 BAG; Product is for Food Service Only; KEEP REFRIGERATED
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0621-2022·2022-02-02

    Sienna Chocolate Decadent Brownie Recalled for Undeclared Pecan

    Dianne's Fine Desserts is recalling Sienna Chocolate Decadent Brownie because it contains undeclared pecan, which poses a risk to consumers with pecan allergies.

    Product
    Sienna Chocolate Decadent Brownie, Net wt. 104 oz. (6-lb. 8 oz.) 2.95 kg., UPC Codes: 8495241115; Product packed in trays covered in clear plastic, trays packed in cardboard case, 4 trays to a case. 1.4 - Unit Size: 6.75 lb tray 1.5 - Container Description: 12 by 16 inch
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-0406-2022·2022-02-02

    Methotrexate Injection Recalled Due to Lack of Sterility Assurance

    Edge Pharma, LLC is recalling Methotrexate, USP, Sterile Solution for Injection (125 mg/5mL) due to lack of assurance of sterility. The recall affects 457 syringes distributed nationwide.

    Product
    Methotrexate, USP, Sterile Solution for Injection (PF), 125 mg/5mL (2mg/mL), 5 mL per syringe, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-1505-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0615-2022·2022-02-02

    Brownie Points Schmurtle Brownies Recalled for Undeclared Peanut Allergen

    Brownie Points LLC is recalling Brownie Points Schmurtle brownies because the label does not disclose peanuts as an allergen. The product was distributed across the United States in gift baskets.

    Product
    Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually
    Category
    Food
    Distribution
    46 states
  • HighCPSC·22067·2022-02-02

    Games Workshop Recalls KOYO Bounca The Squig Plush Toys for Choking Hazard

    Games Workshop is recalling about 2,600 KOYO Bounca The Squig Limited Edition Plush toys because the pom-poms can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    KOYO Bounca The Squig Limited Edition Plush toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0525-2022·2022-02-02

    API ID 32 C Diagnostic Strips Recalled Due to Thermoforming Defect

    Biomerieux is recalling API ID 32 C Strips due to a thermoforming defect that risks misidentification of yeasts or delayed diagnostic results. The recall affects 462 kits in Arizona, Iowa, Kentucky, and New York.

    Product
    API ID 32 C Strips, Reference 32200, Rx Only, IVD API ID 32 C is a qualitative standardized system for the identification of yeasts. It uses miniaturized tests as well as a specially adapted database. After manual inoculation of the strip, reading can be performed either autom
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0524-2022·2022-02-02

    GE Vscan Extend ultrasound device recalled for power-on failure due to battery depletion

    GE Healthcare is recalling the Vscan Extend ultrasound device because it will not power on when the battery is depleted. This occurs when the device is not turned off before battery removal or is connected to a computer without AC power.

    Product
    GE Vscan Extend, being sold as "Vscan Extend Sector Wi-Fi"
    Category
    Medical Device
    Distribution
    50 states
  • HighFDA (Devices)·Z-0515-2022·2022-02-02

    Siemens Diagnostic Angiography System Recalled for Multiple Software Defects

    Siemens is recalling its Artis pheno diagnostic angiography system (12 units) due to four software defects that may prevent imaging, corrupt images, or cause unintended shutdowns during clinical use.

    Product
    Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V046000·2022-02-01

    Jayco Pinnacle and North Point Trailers Recalled for Tire Belt Separation

    Jayco is recalling 2021-2022 Pinnacle and North Point trailers with Sailun tires that may experience belt separation, potentially causing loss of vehicle control. Free tire replacement is available through dealers.

    Product
    JAYCO — 2022 JAYCO PINNACLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V045000·2022-02-01

    Tesla vehicles seatbelt warning chime may fail to activate

    Tesla is recalling vehicles with seatbelt warning chimes that may not activate when the driver has not fastened their seat belt. The fix is a free over-the-air software update.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22718·2022-01-28

    Matrix T1 and T3 Commercial Treadmills Recalled for Fire Hazard

    Johnson Health Tech is recalling about 19,900 Matrix T1 and T3 Series commercial treadmills because the power cord can become loose from the power socket, causing sparking, smoking, melting, and fire. No injuries have been reported.

    Product
    Matrix T1 and T3 Series Commercial Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide