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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20326–20350 of 90018

  • HighFDA (Devices)·Z-1265-2023·2023-03-29

    Attune Revision Limb Preservation System Tibial Insert Recalled for Over-Irradiation

    DePuy Orthopaedics is recalling 7 units of the Attune Revision Limb Preservation System Tibial Insert (Lot JP9022) that received higher than specified gamma radiation doses. The over-irradiation may cause changes to implant material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0641-2023·2023-03-29

    Igarashiseimen Kitakata Spicy Umakara Ramen Recalled for Undeclared Coconut Allergen

    Igarashiseimen Kitakata Spicy Umakara Ramen is being recalled because coconut allergen is not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Igarashiseimen Kitakata Spicy Umakara Ramen UPC: 4967448174211 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0649-2023·2023-03-29

    WHH A&D Calcium Milk Drink Recalled for Undeclared Milk Allergen

    WHH A&D Calcium Milk Drink recalled due to undeclared milk on the ingredient label. The recall affects 12,000 units distributed in California.

    Product
    WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles in 1 pack Made in China
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1264-2023·2023-03-29

    Orthopedic Tibial Insert Recalled Due to Excessive Radiation Exposure

    DePuy Orthopaedics is recalling Attune Revision LPS Tibial Insert devices (Lot JP9016) because they received excessive gamma radiation during manufacturing, which may compromise material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760212
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0472-2023·2023-03-29

    Daytrana methylphenidate patches recalled for defective delivery system

    Noven Pharmaceuticals is recalling Daytrana methylphenidate transdermal patches for a defective delivery system that fails to meet shear specifications. The recall affects specific lots distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1280-2023·2023-03-29

    Wearable ECG smartwatch software bug eliminates physician review

    Withings Scan Monitor/ScanWatch (model hwa09) has a software defect preventing physicians from reviewing ECG recordings, which is critical to the device's FDA clearance requirement for physician-supervised use. Users should discontinue use until the defect is corrected.

    Product
    Scan Monitor/ScanWatch, model number hwa09 Wearable, Bluetooth-connected wrist watch that records heart activity (ECG) and oxygen saturation (SpO2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1284-2023·2023-03-29

    G7 Acetabular Liner Recalled for Size and Label Discrepancy

    Biomet recalled 12 units of its G7 Acetabular System 40mm Size D Liner because the actual implant is a 38mm Size C. The mismatch between outer labeling and the actual implant could result in wrong-size component placement during surgery.

    Product
    G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-0637-2023·2023-03-29

    Meito Milk Cocoa Recalled for Undeclared Coconut Allergen

    Daiso California Warehouse is recalling Meito Milk Cocoa (12gX5P, UPC 4902757444709) because coconut allergen is not declared on the label. Consumers with coconut allergies should discontinue use and return the product.

    Product
    Meito Milk Cocoa 12gX5P (1stick bonus pack) UPC: 4902757444709 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1267-2023·2023-03-29

    DePuy Attune Tibial Insert Recalled for Excessive Radiation Exposure

    DePuy Orthopaedics is recalling Attune Posterior tibial insert implants that received excessive gamma radiation during manufacturing, which may degrade the material properties of the knee replacement component.

    Product
    Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V208000·2023-03-28

    Freightliner Cascadia and Western Star 49X hazard light malfunction recall

    Daimler Trucks North America is recalling 2020-2021 Freightliner Cascadia and Western Star 49X vehicles because hazard warning lights may flash improperly during Advanced Braking Assist events, potentially confusing other drivers and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 49X, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V210000·2023-03-28

    2023 Genesis G90 seat belt pretensioners may explode during crashes

    Hyundai is recalling 575 units of the 2023 Genesis G90 because the seat belt pretensioners may explode in a crash. Metal fragments from the explosion may strike and injure vehicle occupants.

    Product
    GENESIS — GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·011-2023·2023-03-24

    Elkhorn Valley Packing Recalls Boneless Beef Chuck Due to E. coli O103

    Elkhorn Valley Packing is recalling approximately 3,436 pounds of boneless beef chuck product due to possible contamination with Shiga toxin-producing E. coli (STEC) O103.

    Product
    Elkhorn Valley Packing LLC — Elkhorn Valley Packing Recalls Boneless Beef Chuck Product Due to Possible E. coli O103 Contamination
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·23V197000·2023-03-24

    Shadow Living Quarter Trailers Recalled for Gas Leak Risk

    Shadow Trailer is recalling 2016-2023 Living Quarter trailers because cooktop burner tubes may fracture and leak gas, increasing fire risk.

    Product
    SHADOW — SHADOW LIVING QUARTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V202000·2023-03-24

    Forest River Recalls 2023 Pause Travel Trailers Due to Brake Wire Defect

    Forest River is recalling 2023 Pause travel trailers because an incorrectly routed brake wire may pinch, potentially causing brake failure and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER PAUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V201000·2023-03-24

    Forest River Recalls 2023 Pause Travel Trailers Due to Wiring Defect

    Forest River is recalling 2023 Pause travel trailers because a wiring error may prevent the breakaway switch from activating trailer brakes, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER PAUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V198000·2023-03-24

    2023 Ford Edge child restraint system tether welds insufficient

    Ford is recalling certain 2023 Edge vehicles because child seat tether welds may be insufficient, potentially reducing proper child restraint during a crash. Dealers will replace the seat back frame free of charge.

    Product
    FORD — FORD, LINCOLN EDGE, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V200000·2023-03-24

    Mercedes-Benz Recalls 2021 S 580 Vehicles for Water Intrusion Defect

    Mercedes-Benz is recalling 2021 S 580 and Maybach S 580 vehicles because water may enter the passenger compartment, potentially disabling safety features.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V199000·2023-03-24

    Ford Explorer driveshaft disconnect and parking brake recall

    Ford is recalling certain 2020-2022 Explorer vehicles due to potential driveshaft disconnection and incomplete parking brake software, which could cause vehicle rollaway and loss of drive power.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V204000·2023-03-24

    Instrument Cluster Display Failure on 2019-2022 Sprinter Vans Recalled

    Daimler Vans USA is recalling 2019-2022 Mercedes and 2019-2021 Freightliner Sprinters because the instrument cluster may fail to display information. A blank dashboard prevents drivers from seeing speed, fuel level, and warnings, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500, SPRINTER 1500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V203000·2023-03-24

    Jayco Northpoint Fifth Wheel Recall for Axle U-Bolt Tightening Issues

    Jayco is recalling 2023 Northpoint FW travel trailers because improperly tightened axle U-bolts may allow the axle to move, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·010-2023·2023-03-23

    Kelley Foods Recalls Smoked Baby Rope Sausage for Undeclared Milk Allergen

    Kelley Foods is recalling approximately 1,455 pounds of smoked baby rope sausage because the product contains undeclared milk, a known allergen.

    Product
    Keith Valley Packing Company - A Division of Ben E. Keith — Kelley Foods Recalls Smoked Baby Rope Sausage Product Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    2 states