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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20776–20800 of 27460

  • SevereNHTSA·22V817000·2022-11-01

    Brake modulator corrosion recall on Freightliner and Western Star commercial trucks

    Daimler Trucks North America is recalling certain Freightliner Cascadia and Western Star models due to corrosion in front brake modulator valves. The defect may cause brakes to pull to one side during automated braking, increasing crash risk.

    Product
    FREIGHTLINER — 2017 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E092000·2022-11-01

    Tesla 2021 Model S Rearview Mirrors Recalled for Visibility Defect

    Tesla is recalling 2021 Model S exterior rearview mirrors that do not meet federal rear-visibility standards. Defective mirrors may cause drivers to misjudge vehicle distances, raising crash risk.

    Product
    TESLA — 9999 TESLA REARVIEW MIRROR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V818000·2022-11-01

    2017-2021 Tesla Model S and Model X power steering assist loss

    Tesla is recalling 2017-2021 Model S and Model X vehicles due to power steering assist failure on rough roads or after hitting potholes, which increases crash risk.

    Product
    TESLA — 2020 TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V816000·2022-10-31

    2021 Hyundai Santa Fe Hybrid seat belt pretensioners may explode in crash

    Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.

    Product
    HYUNDAI — 2021 HYUNDAI SANTA FE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V814000·2022-10-31

    Tiffin Motorhomes Recall Multiple 2022-2023 Models for LPG Hose Leak Fire Risk

    Tiffin is recalling approximately 295 motorhomes from 2022-2023 because the LPG hose fitting connected to the regulator may leak at the swivel joint, creating a fire hazard in the presence of an ignition source.

    Product
    TIFFIN — 2023 TIFFIN RED 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V815000·2022-10-31

    Volkswagen and Audi Vehicles Recalled for Tire Pressure Monitoring System Failure

    Volkswagen Group of America is recalling 296,044 Volkswagen and Audi vehicles (model years 2019-2021) because the tire pressure monitoring system may fail to detect simultaneous pressure loss in all four tires, increasing crash risk. Dealers will update the TPMS software at no charge.

    Product
    VOLKSWAGEN — 2020 VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23027·2022-10-27

    Goalsetter Wall-Mounted Basketball Goals Recall Due to Detachment Hazard

    Goalsetter is recalling about 18,000 wall-mounted basketball goals because they can detach from walls and fall. One fatality and multiple injuries have been reported.

    Product
    Goalsetter wall-mounted basketball goals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23026·2022-10-27

    Horizon T101-05 Treadmills Recalled for Unexpected Speed and Stop Hazard

    Horizon T101-05 folding treadmills can unexpectedly accelerate, change speed, or stop without user input, posing a fall hazard. About 192,000 units sold in the U.S. are affected; 71 injuries including broken bones have been reported.

    Product
    Horizon T101-05 Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23705·2022-10-27

    LG Energy Solution RESU 10H Batteries Recalled for Fire Hazard

    LG Energy Solution is recalling about 11,500 RESU 10H lithium-ion residential energy storage batteries because they can overheat and pose a fire risk with harmful smoke emissions. One incident of smoking and fire with property damage has been reported.

    Product
    LG Energy Solution "RESU 10H" Lithium-Ion Residential Energy Storage System Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V808000·2022-10-27

    2022 Chrysler 300 and Dodge vehicles TPMS sensor battery failure

    Chrysler and Dodge are recalling certain 2022 models because the tire pressure monitoring system sensor battery may fail prematurely, potentially increasing the risk of tire failure and crashes.

    Product
    CHRYSLER — 2022 CHRYSLER 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23706·2022-10-27

    Punisher Adult Cycling Helmets Recalled Due to Head Injury Risk

    Bike USA is recalling about 3,400 Punisher Adult Cycling Helmets sold online from July 2020 through December 2021. The helmets do not meet safety standards for impact protection and can fail to protect the wearer in a crash.

    Product
    Punisher Adult Cycling Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23704·2022-10-27

    Amazon Basics Executive Desk Chairs Recalled for Fall and Injury Hazards

    Amazon is recalling about 11,400 Amazon Basics Executive Desk Chairs because the leg base can break, creating a fall and injury hazard. The company has received 13 reports of breaking leg bases, including one report of a minor shoulder injury.

    Product
    Amazon Basics Executive Desk Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23025·2022-10-27

    Tesla Cyberquad for Kids ATV Fails Federal Safety Standards

    Radio Flyer is recalling the Tesla Cyberquad for Kids (Model 914) because it violates federal safety standards for youth ATVs and lacks a required CPSC-approved action plan. One incident involving a tip-over has been reported.

    Product
    Tesla Cyberquad for Kids by Radio Flyer, Model Number 914
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23024·2022-10-27

    Brother Recalls Meic Power Adapters for AirSure DF-2 Air Purifiers

    Brother is recalling Meic AC power adapters sold with AirSure DF-2 tabletop air purifiers because the adapter casing can break during plugging or unplugging, exposing metal prongs that pose electrical shock and electrocution hazards.

    Product
    Meic power adapters sold with Brother AirSure DF-2 Dynamic Filtration Tabletop Air Purifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0038-2023·2022-10-26

    Dark Chocolate Almonds recalled for undeclared milk allergen

    Dark Chocolate Almonds sold at Safeway, Albertsons, and Roths Fresh Market contain undeclared milk allergen. The FDA Class I recall affects 1,701 cases distributed in Oregon and Washington.

    Product
    Dark Chocolate Almonds distributed to Safeway/Albertsons is packaged in a clear clamshell container with a top label that displays PRODUCE Dark Chocolate Almonds , net weight of 9.5 oz., UPC 0 19061 19371 2. Distributed by Rivertrail Foods with an address of 4660 Ridge Dr. NE. S
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0075-2023·2022-10-26

    Iso-Gard Filter S Medical Gas Filters Recalled Due to Device Splitting Risk

    TELEFLEX is recalling 355 units of Iso-Gard Filter S medical gas filters nationwide due to incidents of device splitting or detaching during use. The FDA classified this as a Class I recall.

    Product
    Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0074-2023·2022-10-26

    Medical Gas Filter Devices Recalled Due to Splitting and Detachment Risk

    Teleflex is recalling Iso-Gard Filter S microbial medical gas filters that may split or detach during use. The recall affects 164 units distributed nationwide.

    Product
    Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0073-2023·2022-10-26

    Iso-Gard Filter S Medical Gas Filter Recall Due to Splitting or Detachment

    TELEFLEX LLC is recalling Iso-Gard Filter S microbial medical gas filters due to incidents where the device may split or detach during use. The FDA classified this as a Class I recall.

    Product
    Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0080-2023·2022-10-26

    Fenugreek dietary supplement recalled for potential Salmonella contamination

    Best Nutritionals LLC is recalling Best Naturals Fenugreek 610mg capsules due to potential Salmonella contamination. The product was distributed online via internet sellers and FBA.

    Product
    White plastic bottle with green, gold, and blue labeling containing 360, 610mg hard gelatin capsules of Fenugreek seed powder, labeled in part, "Best Naturals Fenugreek Premium Herbal 610mg 3rd Party Lab Tested 360 CAPSULES DIETARY SUPPLEMENT", best by 10/24, lot 102120
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0072-2023·2022-10-26

    Iso-Gard Filter S Recalled for Device Splitting or Detachment During Use

    Teleflex is recalling Iso-Gard Filter S microbial filters (60,500 units) due to incidents of device splitting or detaching during use. The filters protect patients and equipment from bacterial and viral contamination in breathing systems.

    Product
    Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filters for use in breathing system for the protection of patient and equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0076-2023·2022-10-26

    Medical gas filter recalled due to splitting and detachment risk

    TELEFLEX LLC is recalling Iso-Gard Filter S medical gas filters due to incidents of device splitting or detaching during use. The affected filters may compromise patient safety.

    Product
    Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0077-2023·2022-10-26

    Teleflex Catheter Mount and Filter May Split or Detach During Use

    Catheter mounts with filters (REF 191667-000100) used to connect endotracheal tubes or masks to breathing circuits may split or detach during patient use. Teleflex is recalling affected units distributed nationwide.

    Product
    Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube and mask)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0057-2023·2022-10-26

    Lyons Ready Care Thickened Sweet Tea Recalled for Product Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Sweet Tea with Lemon Nectar due to indication of product spoilage. Approximately 491 cases were distributed across all U.S. states.

    Product
    Lyons Ready Care Thickened Sweet Tea with Lemon Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0047-2023·2022-10-26

    Trader Joe's Organic Tortilla Chip Rounds recalled for undeclared milk and soy

    Trader Joe's Organic Yellow Tortilla Chip Rounds may contain undeclared milk and soy allergens. The product contains small amounts of Spicy Cheese Crunchies which were not listed on the label.

    Product
    16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-0449 Distributed and Sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and Sold Exclusively By: Trader Joe's, Monro
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-0097-2023·2022-10-26

    Medical Device Recall: Roche cobas 5800 False Results Due to Baseline Anomalies

    Roche Molecular Systems recalls the cobas 5800 PCR testing instrument due to false positive and invalid results caused by anomalous baselines. This may lead to erroneous or delayed diagnoses.

    Product
    cobas 5800 instrument, Material No. 08707464001. Used for automated Polymerase Chain Reaction (PCR) based Nucleic Acid Testing (NAT) in laboratory settings.
    Category
    Medical Device
    Distribution
    0 states