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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3476–3500 of 113834

  • HighNHTSA·26V187000·2026-03-25

    Aston Martin DBX tire pressure warning light may not illuminate

    Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.

    Product
    ASTON MARTIN — ASTON MARTIN DBX, DBX S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1565-2026·2026-03-25

    Abbott ID NOW influenza test lot shows higher invalid result rates

    Abbott is recalling one lot of the ID NOW Influenza A & B 2 test after confirming the lot has a higher occurrence of invalid rates than stated in the Instructions for Use.

    Product
    Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique Component: Not Applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0391-2026·2026-03-25

    Pitavastatin 2 mg bottle found to contain a 1 mg tablet

    Annora Pharma is recalling one lot of Pitavastatin Tablets 2 mg after one Pitavastatin 1 mg tablet was found in a bottle of 2 mg tablets.

    Product
    PITAVASTATIN CALCIUM — PITAVASTATIN CALCIUM (PITAVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1580-2026·2026-03-25

    Stryker Cub pediatric cribs sold in USA missing two warning labels

    Stryker is recalling Cub Pediatric Cribs, model FL19H, because cribs sold in the USA are missing two access door warning labels.

    Product
    Cub Pediatric Crib, Model FL19H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2026·2026-03-25

    Cardiosave battery charging station left bay screw prevents full battery insertion

    Datascope is recalling the Battery Charging Station, model 0998-00-0802, because a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging.

    Product
    Battery Charging Station; Model: 0998-00-0802;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1574-2026·2026-03-25

    Artegraft vascular graft recalled over incorrect lot outer packaging labeling

    LeMaitre Vascular is recalling one Artegraft Vascular Graft, REF AG740, because of a labeling mix-up resulting in the incorrect lot outer packaging of the product.

    Product
    Artegraft Vascular Graft; REF#: AG740;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0586-2026·2026-03-25

    Wawa Double Dutch Chocolate Milk Recalled for Foreign Plastic Contamination

    Wawa Beverage Company is recalling 5,456 units of Double Dutch Chocolate Milk (16 oz) because foreign plastic material was discovered on the fill line during production.

    Product
    Wawa Double Dutch Chocolate Milk ,16 oz (Pint) Plastic bottle Store Refrigerated
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·H-0578-2026·2026-03-25

    Greenway Farms Jalapeno Dill Pickles Chips Recalled for Safety

    BlueFrog Foods is voluntarily recalling Greenway Farms of Georgia Jalapeno Dill Pickles Chips due to lack of process authority. The product was distributed to one facility in Georgia.

    Product
    GREENWAY FARMS of Georgia JALAPENO DILL PICKLES CHIPS Net Wt 16 fl oz (473 ml) UPC 8 57866 00506 5 Produced by: Greenway Farms of Georgia, LLC Roberta, GA Packed by Blue Frog Food, LLC for Green way Farms of Georgia, LLC 5875 Love St Austell, GA 30168
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0577-2026·2026-03-25

    Greenway Farms Garlic Dill Pickles Chips Recalled for Process Authority

    BlueFrog Foods is voluntarily recalling Greenway Farms of Georgia Garlic Dill Pickles Chips due to lack of process authority. The recall affects one shipment to a facility in Georgia.

    Product
    GREENWAY FARMS of Georgia GARLIC DILL PICKLES CHIPS Net Wt 16 fl oz (473 ml) UPC 8 57866 00501 0 Produced by: Greenway Farms of Georgia, LLC Roberta, GA Packed by Blue Frog Food, LLC for Green way Farms of Georgia, LLC 5875 Love St Austell, GA 30168
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0587-2026·2026-03-25

    Wawa Cookies & Cream Milk recalled for foreign plastic material

    Wawa Beverage Company is recalling Wawa Cookies & Cream Milk (16 oz bottles) due to foreign plastic material discovered on the fill line.

    Product
    Wawa Cookies & Cream Milk 16 oz (Pint), Plastic bottle Store Refrigerated
    Category
    Food
    Distribution
    4 states
  • LowFDA (Food)·H-0569-2026·2026-03-25

    Multivitamin with Fluoride Chewable Tablets Recalled for Subpotent Vitamin D

    Winder Laboratories is recalling Multivitamin with Fluoride Chewable Tablets Grape Flavor because the product contains subpotent Vitamin D levels. The FDA discovered this deficiency during an inspection.

    Product
    Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680
    Category
    Drug
    Distribution
    25 states
  • SevereNHTSA·26V182000·2026-03-24

    Nova Bus driver seat belt tension device may not disengage

    Nova Bus is recalling certain 2016-2023 LFS and LFS Artic transit buses because the driver's seat belt tension-relieving device may fail to disengage without manual intervention. This fails FMVSS 208.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V180000·2026-03-24

    Lexus LX Recall: Front Passenger Air Bag May Deploy Improperly

    Toyota is recalling 2022-2024 Lexus LX vehicles because a seat frame issue may cause the front passenger air bag to deploy incorrectly during a crash.

    Product
    LEXUS — LEXUS LX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V179000·2026-03-24

    2024–2026 Toyota and Lexus vehicles load carrying capacity label incorrect

    Toyota is recalling certain 2024–2026 Toyota and Lexus vehicles because the load carrying capacity modification label may display inaccurate added weight values. Vehicles with incorrect maximum capacity weight may be overloaded, increasing crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4 HYBRID, TACOMA HYBRID, GRAND HIGHLANDER, CROWN SIGNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V177000·2026-03-23

    Winnebago motorhome front turn signal lenses are smaller than required

    Winnebago is recalling certain 2017-2022 Brave, Itasca Sunova, Adventurer and Sunstar motorhomes because the front turn signals may have a smaller than required luminous lens area. This fails FMVSS 108.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ADVENTURER, BRAVE, SUNSTAR, SUNOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03232026-01·2026-03-23

    White Oak Pastures Ground Beef Alerted for Possible Metal Contamination

    USDA FSIS issued a public health alert for White Oak Pastures grassfed ground beef due to possible metal contamination. No injuries have been reported.

    Product
    White Oak Pastures — FSIS Issues Public Health Alert for Ground Beef Products Due to Possible Foreign Material Contamination
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·26V174000·2026-03-20

    Grand Design motorhome steps may deploy unexpectedly while in transit

    Grand Design is recalling certain 2025-2026 Lineage motorhomes because the entry door position switch may not read that the door is closed, allowing the steps to deploy unexpectedly.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V172000·2026-03-20

    Mercedes-Benz Recalls 2026 GLC Models for Rear Seat Belt Defect

    Mercedes-Benz is recalling 2026 GLC models because the center rear seat belts may lack the child seat protection function, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300 4MATIC COUPE, GLC 300, GLC 300 4MATIC, AMG GLC43 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V171000·2026-03-20

    Braun Recalls 2023-2024 Ram ProMaster Vehicles Due to Window Glass Defect

    Braun is recalling 2023-2024 Ram ProMaster vehicles because the installed window may have the wrong type of glass for an emergency exit, increasing the risk of ejection and injury during a crash.

    Product
    BRAUN — BRAUN RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V170000·2026-03-20

    Altec Recalls 2025 Cranes and Derricks Due to Missing Lighting Harness

    Altec is recalling 2025 AC Series Cranes and Digger Derricks because a missing harness may cause loss of body or trailer lights, increasing crash risk.

    Product
    ALTEC — ALTEC AC SERIES CRANE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide