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

Agency

Category

Minimum severity

Clear filters

26526–26550 of 90150

  • HighFDA (Devices)·Z-0708-2022·2022-03-09

    OPAQUE Lacrimal Plugs recalled due to sterile pouch seal defect

    Lacrimedics is recalling approximately 5,767 units of OPAQUE Lacrimal Plugs due to potential defects in the sterile pouch seal that could compromise product sterility. The affected devices were distributed nationwide and internationally.

    Product
    OPAQUE Herrick Lacrimal Plugs, HP3, 0.3 mm, HP5, 0.5mm, HP7, 0.7.mm, STERILE, EO, Rx only, CE Dry eye treatment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0654-2022·2022-03-09

    Digital Angiography System Generators May Emit Excessive X-Ray Radiation

    Shimadzu Medical Systems is recalling Digital Angiography System generators due to potential excessive x-ray radiation in fluoroscopic mode. Installation issues may cause radiation dose rates to exceed safe limits.

    Product
    Digital Angiography System Bransist safire Generator Model D150GC-40
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-0698-2022·2022-03-09

    QC Control Panels Fail Shelf Life Stability Test at 24 Months

    Microbiologics QC control panels for bacterial diagnostic testing failed shelf life validation at 24 months. The 29 affected units were distributed across US states and internationally to Canada, UK, Australia, Belgium, and India.

    Product
    Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and Control Panel. Containing High, Medium and Low Level Controls.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22093·2022-03-09

    Danby Free-Standing and Slide-In Ranges Recalled for Tip-Over Hazard

    Danby is recalling about 1,700 free-standing and slide-in electric and gas ranges because the anti-tip-over bracket may not be securely installed, creating a tip-over hazard and risk of burn injuries when heavy objects are placed on an open oven door.

    Product
    Danby brand free-standing and slide-in electric and gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0707-2022·2022-03-09

    Brasseler K-WIRE surgical instruments recalled for unsealed packaging

    Brasseler USA is recalling 231 units of K-WIRE Double Trocar Smooth surgical instruments due to unsealed packaging that may compromise sterility.

    Product
    Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0685-2022·2022-03-09

    BioPro Titanium Toe Implant Recalled for Incorrect MRI Safety Claims

    BioPro Titanium MPJ toe implants contain incorrect documentation falsely claiming they are MR Conditional without proper testing. Patients should not assume these implants are safe for MRI.

    Product
    Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0803-2022·2022-03-09

    Ice Cream Mislabeled: Black Walnut Packed in Cookie Dough Container

    Signature Select Black Walnut Ice Cream was incorrectly packaged in containers labeled as Cookie Dough, which do not declare nuts as an allergen. The product lid correctly identifies the actual flavor.

    Product
    Signature Select Cookie Dough Ice Cream Vanilla Flavored ice cream with chocolate flavored chips and chunks of chocolaty chip cookie dough. Artificial Flavor added. 1.5 qt. paper container. 6 retail units per case. UPC 2113008803 Some container were filled with Black…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0682-2022·2022-03-09

    Titanium Toe Implant Recalled for Incorrect MR Compatibility Claims

    BioPro Titanium MPJ toe implants are being recalled due to incorrect statements in device labeling claiming MR Conditional status when MR testing was not performed on the titanium version.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0804-2022·2022-03-09

    Carrot Cake Soft Bake Cookies Recalled for Undeclared Pecan Allergen

    J & M Foods is recalling Favorite Day Carrot Cake Soft Bake Cookies because pecans are listed as an ingredient but not declared in the allergen warning statement, posing a risk to consumers with pecan allergies.

    Product
    Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227g) UPC 0 885239 25803 3 packaged in gable top carton 6 units per case
    Category
    Food
    Distribution
    35 states
  • HighFDA (Food)·F-0810-2022·2022-03-09

    Food products from Family Dollar stores recalled due to rodent activity

    Food products from Family Dollar retail stores in six southern states are being recalled due to potential exposure to rodents and rodent activity in a distribution center. Consumers should not consume affected products.

    Product
    Food products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0701-2022·2022-03-09

    Helix Elite Molecular Standards recalled due to shelf life test failure

    Microbiologics Inc is recalling Helix Elite Molecular Standards for Inactivated Influenza A/B and Respiratory Syncytial Virus because shelf life testing failed at 24 months, potentially affecting product stability.

    Product
    Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Influenza A/B and Respiratory Syncytial Virus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0709-2022·2022-03-09

    Lacrimedics Collagen Plugs recalled for potential sterility seal compromise

    Lacrimedics is recalling Collagen Plugs (models CP3, CP4, CP5) due to potential seal integrity defects in sterile pouches. The seals may contain channels that could compromise sterility and allow contamination.

    Product
    Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0714-2022·2022-03-09

    Quality Control Kit Bacterial Strain Shows Unexpected Gentamicin Susceptibility

    Microbiologics has recalled KWIK-STIK quality control kits due to a specific lot failing to meet resistance specifications for Gentamicin Synergy. The affected bacterial strain showed unexpected susceptibility when it should have been resistant.

    Product
    KWIK-STIK, Quality control kit for culture media, sold as: KWIK-STIK (single-pack) Enterococcus faecalis derived from ATCC 51299
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0692-2022·2022-03-09

    AU/DxC AU Magnesium Test Kits Recalled Due to Measurement Error in Lipemic Samples

    Beckman Coulter is recalling 181,776 AU/DxC AU Magnesium test kits because the test may give falsely elevated results in lipemic samples, potentially affecting clinical interpretation.

    Product
    AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
    Category
    Medical Device
    Distribution
    50 states
  • SevereNHTSA·22V136000·2022-03-08

    Triple E Recalls Motorhomes Due to Missing Refrigerator Exhaust Deflectors

    Triple E is recalling 2010-2014 Unity, Libero, and Serenity motorhomes because missing refrigerator exhaust deflectors allow heat to overheat the wood frame, posing a fire risk.

    Product
    TRIPLE E — TRIPLE E SERENITY, LIBERO, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V131000·2022-03-08

    Mercedes-Benz Recalls 2021 Sprinter Vans Due to Torsion Bar Assembly Error

    Daimler Vans USA is recalling 2,153 2021 Mercedes-Benz Sprinter vans because an incorrectly installed shim on the torsion bar may fail, causing loss of vehicle stability and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 3500, SPRINTER 2500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V134000·2022-03-08

    Mercedes-Benz Recalls Metris Vans Due to Fuel Hose Leak Risk

    Daimler Vans USA is recalling 2017-2022 Mercedes-Benz Metris vehicles because insecure fuel hose connections may cause leaks, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V138000·2022-03-08

    Terex Recalls 2016-2021 Aerial Devices Due to Emergency Stop Defect

    Terex is recalling 2016-2021 OM, Optima-HRX, and TCX aerial devices because emergency stop controls may fail to stop all boom functions, increasing injury risk.

    Product
    TEREX — TEREX OPTIMA TCX, OPTIMA HRX, OM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V135000·2022-03-08

    2022 Forest River Cardinal travel trailers recalled for electrical fire risk

    Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.

    Product
    COACHMEN — COACHMEN, FOREST RIVER FREEDOM EXPRESS, CHEROKEE, SABRE, APEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V130000·2022-03-07

    Yamaha Recalls 2021-2022 MT-09 and Tracer 9 GT Motorcycles for ECU Defect

    Yamaha is recalling 2021-2022 MT-09 and Tracer 9 GT motorcycles because improper ECU programming may cause engine stalls or limit throttle response, increasing crash risk.

    Product
    YAMAHA — YAMAHA MT-09, TRACER 9, TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V132000·2022-03-07

    Ubco Recalls 2021-2022 2X2 ADV Motorcycles Due to Wheel Hub Gear Defect

    Ubco is recalling 2021-2022 2X2 ADV motorcycles because a wheel hub gear may loosen and contact the motor, potentially causing the wheel to seize and increasing crash risk.

    Product
    UBCO — UBCO 2X2 ADV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2022·2022-03-04

    Boyd Specialties Recalls Jerky Products Due to Possible Listeria Contamination

    Boyd Specialties is recalling approximately 1,634 pounds of ready-to-eat jerky products due to possible Listeria monocytogenes contamination. The products were shipped to retail locations in eight states.

    Product
    Boyd Specialties LLC — Boyd Specialties, LLC Recalls Jerky Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·22V125000·2022-03-04

    Mercedes-Benz Recalls 2020-2021 Models for Rear Brake Caliper Fastener Issue

    Mercedes-Benz is recalling 2020 AMG CLA 35 and 2021 GLA 250 vehicles because loose rear brake caliper fasteners may reduce braking performance or cause parts to detach.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250, AMG CLA35
    Category
    Vehicle
    Distribution
    Distributed nationwide