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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

22401–22425 of 114376

  • HighFDA (Devices)·Z-2101-2023·2023-07-12

    Giraffe OmniBed neonatal incubator recall due to incorrect secondary latch installation

    GE HealthCare is recalling Giraffe OmniBed neonatal incubators with potentially incorrect secondary latches on bedside panels. An incorrect latch type may have been installed on northeast and/or northwest panels of affected units.

    Product
    Giraffe OmniBed, with the following Model Numbers: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, 6650-0094-901, 6650-0001-9901, 6650-0029-901, 6650-0080-901, 6650-0032-901, 6650-0077-901, 6650-001-901, 6650-0006-901, 6650-0129-901, 6650-0063-902, 6650-0130-901…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2071-2023·2023-07-12

    SurgiMend collagen matrices recalled for endotoxin test result quality issues

    TEI Biosciences recalls SurgiMend 1.0 collagen matrices due to problems with endotoxin testing procedures that may have produced inaccurate test results. 52 units were distributed nationwide.

    Product
    SurgiMend 1.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 18x12 cm Thin and 10x15 cm Thin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0894-2023·2023-07-12

    Tizanidine tablets recalled nationwide for failed stability specifications

    Preferred Pharmaceuticals is recalling 541 bottles of Tizanidine 4mg tablets nationwide due to failed stability specifications. Consumers with affected lot numbers should contact their pharmacist or healthcare provider.

    Product
    TIZANIDINE — TIZANIDINE (TIZANIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2095-2023·2023-07-12

    Teleflex Pilling O'Reilly Esophageal Retractor Recalled for Incomplete Cleaning Instructions

    TELEFLEX LLC recalled the Pilling O'REILLY ESOPHAGEAL RETRACTOR (REF 381801A) due to incomplete pre-cleaning instructions in the product's Instructions for Use. The recall affects 365 units distributed nationwide and internationally.

    Product
    Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2092-2023·2023-07-12

    NexGen Tibial Plate Recalled for Incorrect Outer Packaging Label

    Zimmer, Inc. is recalling NexGen Precoat Stemmed Tibial Plate Size 5 devices due to incorrect outer packaging labeling. Affected units were distributed internationally in India.

    Product
    NexGen Precoat Stemmed Tibial Plate Size 5
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2084-2023·2023-07-12

    Collagen matrix recalled for endotoxin testing methodology issues

    TEI Biosciences recalled 665 units of Revize-X collagen matrix nationwide due to possible out-of-specification endotoxin test results caused by issues with the company's testing procedures. No illnesses have been reported.

    Product
    Revize-X; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 12x6 cm and 10x9 cm.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0892-2023·2023-07-12

    Prescription Drug Tizanidine Tablets Recalled for Failed Dissolution Specifications

    Amerisource Health Services LLC recalls approximately 4,971 cartons of Tizanidine Tablets due to failed dissolution specifications. Tablets that do not dissolve properly may not provide intended therapeutic benefit.

    Product
    TIZANIDINE — TIZANIDINE (TIZANIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2096-2023·2023-07-12

    Teleflex Surgical Retractor Recalled for Incomplete Pre-Cleaning Instructions

    Teleflex LLC is recalling 170 units of the Pilling Lowsley Prostatic Retractor due to incomplete pre-cleaning instructions in the user manual. Incomplete instructions may prevent proper sterilization of the surgical instrument.

    Product
    Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2093-2023·2023-07-12

    COVID-19 Test Strips Recalled for Lot Number Label Discrepancy

    NeuMoDx SARS-CoV-2 test strips from lot 123909 have conflicting lot numbers between the package label and barcode label that the instrument reads.

    Product
    NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2098-2023·2023-07-12

    KLS Martin Battery Packs Recalled for Switched Expiration Date Labels

    Pro-Dex Inc recalls KLS Martin Battery Packs used in surgical screwdrivers due to manufacturing and expiration dates being reversed on sterile pouch labels, causing batteries to appear prematurely expired.

    Product
    KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·23V474000·2023-07-11

    Prevost H3-45 Turn Signal Light Failure Increases Crash Risk

    Prevost is recalling 2022-2024 H3-45 and H3-45 VIP vehicles because the right front turn signal light may fail when activated. Inoperative turn signals and hazard lights reduce visibility to other drivers and increase crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V475000·2023-07-11

    Prevost Recalls X3-45 Commuter Buses Due to Seat Bolt Loosening

    Prevost is recalling 2021 and 2023 X3-45 Commuter buses because a seat bolt may loosen, leaving the seat back unsecured and increasing crash injury risk.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V485000·2023-07-11

    2023 Toyota RAV4 Recalled for Improperly Installed Tire Valve Stems

    Gulf States Toyota is recalling 195 2023 Toyota RAV4 vehicles equipped with 17" black alloy wheels. The tire valve stems may be improperly installed or damaged, potentially causing air leakage, underinflation, and crash risk.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V473000·2023-07-10

    Boreas Camper XT Travel Trailers Recalled for Gas Leak Risk

    Boreas Campers is recalling 2021-2022 XT travel trailers because a cooktop component may fracture and cause a gas leak, increasing fire risk.

    Product
    BOREAS CAMPER — BOREAS CAMPER XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V471000·2023-07-10

    2023 BMW XM and 2024 X5-X7 vehicles recalled for knee air bag defect

    BMW of North America is recalling 2023 XM and certain 2024 X5, X6, and X7 vehicles because the knee air bag may not have been manufactured correctly and could fail to deploy during a crash. Dealers will replace the air bag free of charge.

    Product
    BMW — BMW X5, X6, XM, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E052000·2023-07-10

    Dana Spicer Driveshafts Recalled for Risk of Breaking Under Load

    Dana Incorporated is recalling specific Dana-Spicer driveshafts that can break under certain loading conditions, potentially causing a loss of drive power and increasing crash risk.

    Product
    POWER TRAIN:DRIVELINE:DRIVESHAFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V468000·2023-07-07

    2023 Toyota Tundra Spare Tire Carrier May Detach Due to Insufficient Welds

    Toyota is recalling certain 2023 Tundra, Tundra Hybrid, and Sequoia Hybrid vehicles due to insufficiently welded spare tire carrier assemblies that may break and allow the spare tire to detach, increasing crash risk.

    Product
    TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA, SEQUOIA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V469000·2023-07-07

    Newmar motorhomes recalled for defective seat belt mounting brackets

    Newmar is recalling certain 2019–2023 motorhomes because modified seat belt mounting brackets can fail to properly restrain occupants in a crash, violating federal safety standards.

    Product
    NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT, SUPER STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V467000·2023-07-06

    Freightliner Recalls eCascadia Trucks for E-Axle Welding Defect

    Daimler Trucks is recalling 2023-2024 Freightliner eCascadia vehicles because a defective e-axle weld may cause sudden loss of drive power, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER E-CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23238·2023-07-06

    VRURC Portable Chargers Recalled Due to Fire Hazard

    VRURC portable chargers (model OD-B7) sold on Amazon.com from July 2021 through May 2023 can ignite and pose a fire hazard. One charger caught fire on a commercial flight, injuring four flight attendants.

    Product
    VRURC portable chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23239·2023-07-06

    woom ORIGINAL Kids' Bicycles Recalled Due to Fall Hazard

    woom Bikes USA recalls about 84,000 woom ORIGINAL children's bicycles from model years 2018–2021. The stem and handlebar can detach, causing riders to lose control and fall.

    Product
    woom ORIGINAL Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23772·2023-07-06

    Yamaha Model Year 2023 Golf Cars and PTVs Recalled for Crash and Death Hazards

    Yamaha is recalling about 11,000 Model Year 2023 Golf Cars, Personal Transportation Vehicles, and Umax models because the accelerator spring can become dislodged, preventing the accelerator pedal from returning to rest and posing crash, injury, and death hazards.

    Product
    Model Year 2023 Yamaha Golf Car, Personal Transportation Vehicles (PTV) and Umax
    Category
    Vehicle
    Distribution
    Distributed nationwide