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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14901–14925 of 89769

  • HighFDA (Devices)·Z-0844-2024·2024-02-07

    Surgilon Braided Nylon Sutures Recalled for Excessive Gamma Sterilization

    Covidien LP recalls specific lots of Surgilon Braided Nylon sutures sterilized with excessive gamma radiation, which may weaken the sutures and cause wound complications.

    Product
    Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT 88861919-51 SURGILON* 2-0 BLK 7X75CMPCT 88861919-71 SURGILON* 1 BLK 7X75CM PCT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0903-2024·2024-02-07

    Howmedica Osteonics Trident Knee Insert Recalled for Oxidation Risk

    Howmedica Osteonics Trident knee replacement inserts manufactured with raw material over 5 years old may have elevated oxidation levels affecting material properties. This FDA Class II recall applies to Lot Number 29518001.

    Product
    HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0880-2024·2024-02-07

    Knee Replacement Implant Recalled for Potential Material Degradation Risk

    Howmedica Osteonics Corp. is recalling SCORPIO TS TIB knee replacement implants manufactured with aged raw material that may develop oxidation, potentially affecting performance.

    Product
    SCORPIO TS TIB INSERT. Intended for knee replacement Part Number: 72-4-7518
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0818-2024·2024-02-07

    Cardiac surgical kits recalled due to improper sterilization exposure

    American Contract Systems is recalling 12,291 cardiac procedure kits nationwide. Components were exposed to sterilization without documented assessment of suitability, potentially causing loss of functionality or efficacy.

    Product
    Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB DEVICE IMPLANT, kit number AGDI40J; c) LAB DEVICE IMPLANT, kit number AGDI40K; d) MINOR VASCULAR, kit number AGMV26O; e) OPEN HEART ACCESSORY, kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0829-2024·2024-02-07

    Obstetrical Labor and Delivery Kits Recalled for Potential Functionality Loss

    American Contract Systems has recalled Labor and Delivery Packs because certain components may have lost functionality or efficacy due to unvalidated sterilization exposure.

    Product
    Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LABOR & DELIVERY PACK, kit number HILD52F; b) LABOR & DELIVERY PACK, kit number HILD52G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0860-2024·2024-02-07

    Philips Azurion 7 M20 FlexArm system recalled for software connectivity loss

    Philips Medical Systems recalls the Azurion 7 M20 FlexArm system due to a software issue causing loss of connectivity between the FlexArm and Maquet Magnus Table. The recall affects 28 systems worldwide.

    Product
    Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0284-2024·2024-02-07

    Rifampin Antibiotic Capsules Recalled for Subpotency and Failed Specifications

    Lupin Pharmaceuticals recalls Rifampin 300mg capsules (lot A200817, exp 1/2024) due to subpotency and failed impurities/degradation specifications. Patients should consult their doctor before stopping medication.

    Product
    RIFAMPIN — RIFAMPIN (RIFAMPIN)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0882-2024·2024-02-07

    SCORPIO TS TIB INSERT Knee Replacement Components Recalled for Potential Material Degradation

    Howmedica Osteonics is recalling SCORPIO TS TIB INSERT knee replacement inserts manufactured with aging raw material. The material may develop elevated oxidation that could affect performance.

    Product
    SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7524
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0924-2024·2024-02-07

    Knee Replacement Insert May Degrade from Oxidized Raw Material

    Howmedica Osteonics is recalling PS LIPPED TIBIAL INSERT ASSY DURACON knee replacement inserts manufactured with UHMWPE raw material over 5 years old. The aged material may develop elevated oxidation that could impact material properties.

    Product
    PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0914-2024·2024-02-07

    Knee Replacement Inserts Recalled Due to Potential Material Degradation

    Howmedica Osteonics is recalling PRIMARY REV.TIB.INSERT-DURACON knee replacement inserts manufactured with aging UHMWPE material that has potential for oxidation affecting material properties. Affected lots: 36273601 and 36609701.

    Product
    PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0894-2024·2024-02-07

    SCORPIO U-Dome Patella Knee Implant Recalled Due to Material Degradation Risk

    Howmedica Osteonics has recalled certain SCORPIO U-Dome Patella knee implants due to potential material oxidation in units manufactured with raw material over 5 years old. The oxidation may affect the implant's material properties.

    Product
    SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V072000·2024-02-06

    Mitsubishi Fuso Rizon Trucks Recalled for Unexpected Drive Power Loss

    Mitsubishi Fuso is recalling 2024 Rizon FEC7K and FEC9K trucks because a control unit error may cause the vehicle to shut down unexpectedly, increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC7K (E16), RIZON FEC9K (E18)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E007000·2024-02-05

    Worldwide Recalls INGUSA/LP ASME Remote Fill Tanks Due to Leak Risk

    Worldwide Distribution is recalling INGUSA/LP ASME Remote fill tanks because the liquid level remote fill gauge may leak in the open position, increasing fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:TANK VALVE/GAUGE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·005-2024·2024-02-03

    Hormel Recalls Spiced Deli Ham for Undeclared Milk Allergen

    Hormel Foods is recalling approximately 945 pounds of ready-to-eat spiced deli ham products due to misbranding and an undeclared milk allergen. The products were distributed to retail locations in Pennsylvania.

    Product
    Hormel Foods Corporation — Hormel Foods Recalls Ready-To-Eat Spiced Deli Ham Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·004-2024·2024-02-02

    Macgregors Recalls Frozen Ready-to-Eat Pork Products for Import Violation

    Macgregors Meat and Seafood Ltd is recalling approximately 2,745 pounds of frozen, ready-to-eat pork products that were imported into the U.S. without required reinspection.

    Product
    Macgregors Meat and Seafood Ltd Recalls Frozen Ready-To-Eat Pork Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·24V069000·2024-02-02

    Indian Challenger and FTR Motorcycles Recalled for Unintended Brake Light Illumination

    Indian Motorcycle Company is recalling certain 2019-2022 Challenger, FTR 1200, and Pursuit motorcycles due to brake lights that may illuminate unexpectedly without rider input, potentially confusing following drivers and increasing crash risk.

    Product
    INDIAN — INDIAN PURSUIT DARK HORSE, FTR 1200 S, FTR1200, CHALLENGER LIMITED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V068000·2024-02-02

    Blue Bird Recalls 2021-2024 Vision School Buses for Stop Arm Defect

    Blue Bird is recalling 2021-2024 Vision school buses because a software defect may cause warning lights to turn off and the stop arm to retract unexpectedly.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V066000·2024-02-02

    Forest River Salem and Wildwood travel trailers incorrect tire size

    Forest River is recalling 2023-2024 Salem and Wildwood fifth wheel travel trailers due to incorrect tire size information on their federal placards. This could lead to wrong tire installation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V070000·2024-02-02

    2019-2022 Mercedes-Benz GLC models recalled for incorrect headlight adjustment and glare

    Mercedes-Benz is recalling 2019-2022 GLC 300, 2020 GLC 350e, and 2020-2022 AMG GLC 43 vehicles for headlights that may be incorrectly adjusted, creating glare for oncoming traffic. Dealers will correct the adjustment free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC43, GLC 300, GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V071000·2024-02-02

    Nissan LEAF rearview camera harness damage reduces rear visibility

    Nissan is recalling approximately 57,914 LEAF vehicles (2018-2022) where the rearview camera harness may become damaged, causing image distortion or loss and reducing rear visibility.

    Product
    NISSAN — NISSAN LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V067000·2024-02-02

    Gulf Stream Trail Boss Trailers Recalled for Incorrect Tire Labeling

    Gulf Stream is recalling 2024 Trail Boss 160FK trailers because the federal certification label lists incorrect tire size and pressure, which could lead to improper tire installation.

    Product
    GULF STREAM — GULF STREAM TRAIL BOSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24096·2024-02-01

    Fishing Games Recalled for High-Powered Magnet Ingestion Hazard

    Huihuang Trading is recalling Fishing Games sold on Amazon.com from June through July 2023 because they contain magnets that exceed federal safety limits. Swallowed magnets can become lodged in the digestive system and cause serious injury or death.

    Product
    Fishing Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24097·2024-02-01

    DailySale Magnetic DIY Balls Magic Cube Recalled for Ingestion Hazard

    DailySale Inc. is recalling its 216-piece 5mm Magnetic DIY Balls Magic Cube because the high-powered magnets violate federal toy safety regulations. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Magnetic DIY Balls Magic Cube, 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide