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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19251–19275 of 114351

  • HighFDA (Food)·F-0577-2024·2023-12-20

    Greek Feta Dressing and Related Products Recalled for Temperature Abuse

    Ben E Keith Foods is recalling Greek Feta dressing and other refrigerated and frozen foods shipped in a temperature-abused trailer, affecting 1,721 cases total. No illnesses have been reported.

    Product
    DRESSING GREEK FETA
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0504-2024·2023-12-20

    Tyson 2.0 Kava and Kratom Supplement Recalled for Unapproved Additive and pH Control Failure

    LGNDS LLC is recalling TYSON 2.0 Kava & Kratom Blend because the product contains kratom, an unapproved food additive, and has a pH level exceeding the required maximum for acidified products.

    Product
    TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, Mocha, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Kratom Leaf Extract (30%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583608, POWERED BY LGNDS, 12 bottles of 2oz each per…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0661-2024·2023-12-20

    Gaw's Salami & Cheese Bagel recalled for undeclared sesame allergen

    Gaws Gourmet Foods is recalling Gaw's Salami & Cheese Bagel 6oz due to undeclared sesame allergen. Affected products have use-by dates from November 28 through December 15, 2023.

    Product
    Gaw's Salami & Cheese Bagel 6oz, Foam Tray with Clear Plastic Wrap package, UPC:1725600501
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0547-2024·2023-12-20

    Laboratory Diagnostic System Software Malfunction Causes System Freezes and Delays

    Ortho-Clinical Diagnostics recalls 216 VITROS XT 7600 laboratory systems running Software Version 3.8.0 due to software issues causing screen freezes and unresponsiveness. The defects delay test result reporting and could postpone patient treatment.

    Product
    VITROS XT 7600 Integrated System Product Code 6844461 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0534-2024·2023-12-20

    Medline Leg Bags Recalled Due to Undeclared Latex

    Medline Industries has recalled approximately 19,406 leg bags due to undeclared latex. Patients with latex allergies may experience allergic reactions from skin contact with the device.

    Product
    Medline Leg bag, REF DYND12578
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0546-2024·2023-12-20

    Chemistry System Software Malfunction Causes Freezes and Result Reporting Delays

    Ortho-Clinical Diagnostics is recalling VITROS XT 3400 Chemistry Systems due to software issues causing screen freezes and system unresponsiveness. The problems can delay reporting of patient test results, including critical or STAT assays.

    Product
    VITROS XT 3400 Chemistry System Product Code 6844458 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0530-2024·2023-12-20

    Non-sterile Betadine solution labeled and distributed as sterile

    Medline Industries is recalling 1,800 units of Sterile Betadine (Ref DYNDA1998) because the foil sachet contents are non-sterile, despite labeling that claims sterility. The recall affects units nationwide in eight states.

    Product
    STERILE BETADINE, REF DYNDA1998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0521-2024·2023-12-20

    Cardinal Health Stool Transportation System Recalled for Vial Leakage

    Meridian Bioscience is recalling the Cardinal Health Clean Stool Transportation System due to a manufacturing defect that may cause Para-Pak vials to leak. Affected product: 38 cases with Lot Number 510020Q, distributed nationwide and to Italy.

    Product
    Cardinal Health Clean Stool Transportation System-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: CHB900312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0573-2024·2023-12-20

    Frozen and Refrigerated Cheese Products Recalled Due to Temperature Abuse

    Ben E Keith Foods - Fort Worth is recalling frozen and refrigerated cheese products that were subjected to temperature abuse during storage and transport.

    Product
    CHEESE VELVEETA LOAF; CHEESE CHEDDAR SLICE MILD; CHEESE STICK MOZZ BATTERED; CHEESE CHEDDAR SLICE MILD
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0517-2024·2023-12-20

    Brachytherapy Treatment Planning Software Recalled Due to Measurement Inaccuracy

    SagiPlan 2.2 brachytherapy treatment planning software is recalled due to a software malfunction that may round numerical values, potentially causing inaccurate treatment measurements.

    Product
    SagiPlan 2.2, CE0344, Rx Only , Brachyterapy Treatment Planning System
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0602-2024·2023-12-20

    Deli Club Sandwich Recalled Due to Inaccurate Label Information

    E.A. Sween Co. is recalling Deli Express Deli Club sandwiches (lot U023236) due to label mix-up with inaccurate required label information. The recall affects 31,550 units distributed across 19 states.

    Product
    Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157
    Category
    Food
    Distribution
    19 states
  • ModerateFDA (Devices)·Z-0509-2024·2023-12-20

    Spectranetics Turbo-Elite Atherectomy Catheters recalled due to labeling mismatch

    Spectranetics Corporation is recalling 1,239 Turbo-Elite Laser Atherectomy Catheters due to incorrect labeling where the exterior product box label does not match the internal pouch label.

    Product
    Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 OTW REF 420-006 Spectranetics Turbo-Elite Laser Atherectomy Catheter 1.4 RX REF 414-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0506-2024·2023-12-20

    Hungry Root Marinara Sauce recalled for yeast and mold contamination

    BC Gourmet USA, Inc. is recalling 81,312 units of Hungry Root Marinara Sauce due to yeast and mold contamination. Affected products were distributed in California, New Jersey, and Indiana.

    Product
    Hungry Root Marinara Sauce; 10.5 oz Plastic Cup; UPC 81006252077
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0572-2024·2023-12-20

    Frozen and Refrigerated Foods Recalled Due to Temperature Abuse

    Ben E Keith Foods recalls approximately 1,721 cases of frozen and refrigerated food products due to temperature abuse during distribution to food services.

    Product
    MILK HOMO GALLON
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0576-2024·2023-12-20

    Frozen Bread Products Recalled Due to Temperature Abuse During Shipment

    Ben E Keith Foods recalls 1721 cases of frozen bread products that experienced temperature abuse during truck shipment to food services. Products include sandwich bread, dinner rolls, and hamburger buns.

    Product
    BREAD SANDWICH WHITE LOAF, ROLL DINNER HAWAIIAN, BUN HAMBURGER WHITE 4.5 IN FZN
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0150-2024·2023-12-20

    Liothyronine Sodium tablets recalled due to failed impurity and degradation specifications

    Sun Pharmaceutical is recalling 96,192 bottles of Liothyronine Sodium Tablets nationwide due to failed quality specifications for impurities and degradation. The affected lots were distributed in 100-count bottles.

    Product
    LIOTHYRONINE SODIUM — LIOTHYRONINE SODIUM (LIOTHYRONINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0507-2024·2023-12-20

    Hungry Root Creamy Vodka Sauce Recalled for Yeast and Mold Contamination

    BC Gourmet USA is recalling Hungry Root Creamy Vodka Sauce (10.5 oz Plastic Cup) due to the presence of yeast and mold. The affected product was distributed in California, New Jersey, and Indiana.

    Product
    Hungry Root Creamy Vodka Sauce; 10.5 oz Plastic Cup; UPC 810062520787
    Category
    Food
    Distribution
    3 states
  • LowFDA (Devices)·Z-0556-2024·2023-12-20

    Medical Device Instructions Update Recall for Navik 3D Mapping System

    APN Health LLC is recalling the Navik 3D v2 3D Mapping System to update the product instructions for use. The firm initiated this voluntary recall.

    Product
    Navik 3D v2, REF NAVIK3D, 3D Mapping System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V862000·2023-12-19

    2022-2023 Tesla Model S and X Door Latch Safety Defect Recall

    Certain 2022-2023 Tesla Model S and X vehicles may have cabin doors that unlock during a crash due to a door latch defect. Tesla is providing a free over-the-air software update to fix the issue.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V861000·2023-12-19

    Van Hool Recalls 2024 CX45 Vehicles Due to Seat Belt Screw Defect

    Van Hool is recalling 64 2024 CX45 vehicles because a seat belt assembly screw may break. This defect could prevent the seat belt from properly restraining occupants during a crash.

    Product
    VAN HOOL — VAN HOOL CX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V859000·2023-12-19

    Doosan Portable Generator Trailers Recalled for Brake Wiring Defect

    Doosan is recalling 2019-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, causing brakes to fail when the battery switch is off.

    Product
    DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V860000·2023-12-19

    Airstream Basecamp Travel Trailers Recalled for Failing Spare Tire Bracket

    The spare tire carrier bracket on certain 2012-2023 Airstream Basecamp travel trailers may experience metal fatigue and break, causing the spare tire to detach and become a road hazard. Airstream is providing free replacement and reinforcement of the bracket.

    Product
    AIRSTREAM — AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V858000·2023-12-18

    Fuel pump failure recall for 2013-2023 Honda and Acura vehicles

    Honda is recalling certain 2013-2023 Honda Accord, Civic, CR-V, HR-V, Odyssey, Pilot, Ridgeline and Acura ILX, MDX, RDX, RLX, TLX vehicles because the fuel pump inside the fuel tank may fail, potentially causing engine stall while driving and increasing crash risk.

    Product
    HONDA — HONDA, ACURA CIVIC TYPE R, CLARITY PLUG-IN HYBRID, ACCORD, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide