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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22601–22625 of 26068

  • HighFDA (Devices)·Z-0642-2022·2022-02-23

    Dental Resin Product Recalled Due to Non-Registered Manufacturing and Mislabeling

    Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.

    Product
    FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0638-2022·2022-02-23

    Endoscope Reprocessor Tubing Assembly Error May Reduce Disinfection Effectiveness

    Olympus OER-Elite Endoscope Reprocessors may have incorrectly assembled detergent and alcohol tank tubing, causing solutions to be dispensed in reversed cycles. This results in ineffective endoscope disinfection and potential patient exposure to residual detergent.

    Product
    OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes, their accessories, and endoscope reprocessor accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0640-2022·2022-02-23

    Liko Mobile Patient Lifts Recalled for Missing Bushings and Wear Risk

    Hill-Rom is recalling 1,215 Liko M220 and M230 mobile patient lifts with missing bushings that cause wear and risk of patient falls. Units were distributed worldwide.

    Product
    Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0646-2022·2022-02-23

    Destino Twist and Guidestar Devices Recalled for Potential Threaded Component Separation

    Oscor Inc. is recalling 549 units of Destino Twist and Guidestar devices due to potential separation between the threaded hub and cap. Affected devices were distributed in Tennessee, Pennsylvania, and the Czech Republic.

    Product
    Destino Twist 14F (also branded as Guidestar 14F)
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·22V105000·2022-02-23

    2022 Keystone Cougar Tires: Load Range Defect Increases Crash Risk

    Keystone RV recalls 2022 Cougar trailers with incorrectly specified tires. Load Range D tires were installed instead of required Load Range E, creating overload and crash risk.

    Product
    KEYSTONE — 2022 KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0736-2022·2022-02-23

    Pretty Thai Sweet Chili Sauce Recalled for Undeclared Peanuts

    Pretty Thai Sweet Chili Stir Fry & Barbecue Sauce is being recalled due to potential undeclared peanuts. Consumers with peanut allergies should not consume the product.

    Product
    Pretty Thai Sweet Chili Stir Fry & Barbecue Sauce NET WT. 11.2 oz (317g) UPC 860043001224 packaged in a cylindrical clear PET plastic bottle
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0644-2022·2022-02-23

    Howmedica Osteonics Medical Device Packaging Defect: Tyvek Lid De-bonding Recall

    Howmedica Osteonics is recalling medical devices because the outer Tyvek lid may separate from the package seal. This affects 32MM -4 V40 TAPER VIT HEAD devices distributed worldwide.

    Product
    32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0734-2022·2022-02-23

    Organic Roasted Salted Cashews Recalled for Mislabeled Hazelnuts

    Honey Heaven Wholesale Inc is recalling Organic Roasted Salted Cashews because the product contains hazelnuts but is labeled as cashews. Hazelnuts are visible through the package window.

    Product
    Organic Roasted Salted Cashews, Net Weight of 6 oz (170g), UPC 6 16316 76283 1. Product is packed in a brown kraft stand-up paper pouch with plastic front viewing window with a zip-lock top that was heat sealed to close. The labeled cashew package has the ingredient statement
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0648-2022·2022-02-23

    Philips Zenition 70 Wireless Foot Switch Firmware Failure Recall

    Philips is recalling Zenition 70 wireless foot switches due to a firmware issue that can cause the device to stop responding. This could interrupt imaging procedures if alternative controls are not used.

    Product
    Zenition 70, Model #718133
    Category
    Medical Device
    Distribution
    26 states
  • HighCPSC·22086·2022-02-23

    Festive Lights Hanukkah Menorahs Recalled Due to Fire Hazard

    The TJX Companies is recalling about 7,900 Festive Lights Hanukkah Menorahs because the resin and MDF material can burn or catch fire when holding lit candles. Three incidents of burning or catching fire have been reported, with no injuries or property damage.

    Product
    Festive Lights Hanukkah Menorahs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0649-2022·2022-02-23

    Wireless Foot Switch Firmware Issue in Philips Veradius Unity Devices

    The wireless foot switch in Philips Veradius Unity medical systems can lose function due to a firmware issue. This could cause delays or interruption of medical procedures if alternative input methods are not used.

    Product
    Veradius Unity, Model #718132
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0651-2022·2022-02-23

    Exeter V40 Cemented Hip Stem Recalled for Potential Label Mix-Up

    Howmedica Osteonics is recalling Exeter V40 Cemented Hip (125mm) Stem devices due to a potential label mix with 150mm stems. Incorrect labeling could result in wrong implant size being used during surgery.

    Product
    Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0652-2022·2022-02-23

    Exeter V40 Cemented Hip Stem Labels May Mismatch Between Sizes

    The FDA has recalled Exeter V40 Cemented Hip (150mm) Stems due to a potential labeling mix-up with the 125mm version. Patients who received the device should verify with their surgeon that the correct size was implanted.

    Product
    Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
    Category
    Medical Device
    Distribution
    1 state
  • HighCPSC·22087·2022-02-23

    Bebe au Lait Wooden Teethers Recalled for Choking Hazard

    Bebe au Lait is recalling approximately 8,600 wooden teethers because the string connecting beads can come untied, releasing beads that pose a choking hazard to young children. The company has received six reports of detached beads, including one case where a child placed a bead in their mouth.

    Product
    Wooden Teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0639-2022·2022-02-23

    Liko M220 mobile lifts recalled for missing bushing, fall risk

    Hill-Rom is recalling 5,470 Liko M220 mobile lifts used in nursing homes due to a missing bushing that can cause wear and potentially lead to patient falls.

    Product
    Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V100000·2022-02-22

    2021 Porsche Taycan: Center Seat Belt Buckle May Block Child Seat Anchors

    Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.

    Product
    PORSCHE — 2021 PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V101000·2022-02-22

    2022 Freightliner Cascadia brake system failure and parking brake defect

    Daimler Trucks North America is recalling 2022 Freightliner Cascadia trucks for a software and brake hardware defect that may cause loss of braking and parking brake functionality, increasing crash risk.

    Product
    FREIGHTLINER — 2022 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V091000·2022-02-17

    2022 Chevrolet Corvette rear driveshaft defect may cause loss of power

    General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.

    Product
    CHEVROLET — 2022 CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22725·2022-02-17

    BrushX Hot Air Brushes Recalled for Electrocution Hazard

    Ecom Brands has recalled approximately 100,000 BrushX hot air brushes due to lack of immersion protection, creating an electrocution or shock hazard if the device falls into water while plugged in. No injuries have been reported.

    Product
    Hot Air Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22729·2022-02-17

    Polaris Model Year 2022 Snowmobiles Recalled for Crash Hazard

    Polaris Industries is recalling approximately 7,400 Model Year 2022 MATRYX snowmobiles because the throttle release switch can fail to disengage or the throttle cable can be kinked, posing a crash hazard.

    Product
    Model Year 2022 MATRYX RMK, INDY, SWITCHBACK, VOYAGEUR, and NORDIC PRO snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22727·2022-02-17

    Husqvarna All-Wheel Drive Robotic Lawnmowers Recalled for Fire Hazard

    Husqvarna is recalling about 1,400 Automower 435X and 535 all-wheel drive robotic lawnmowers because the lithium-ion battery can overheat and catch fire. The company has received five reports of battery overheating, including two fires.

    Product
    Husqvarna Automower 435X and 535 All-Wheel Drive Robotic Lawnmowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22726·2022-02-17

    Yamaha Golf Cars and Personal Transportation Vehicles Recalled for Brake Failure

    Yamaha is recalling approximately 5,000 golf cars and personal transportation vehicles from model years 2021 and 2022 because they can experience brake failure, creating a crash hazard that could cause injury or death.

    Product
    Yamaha Golf Cars and Personal Transportation Vehicles (PTV)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22728·2022-02-17

    H&M Children's Sleepwear Sets Violate Federal Flammability Standards

    H&M is recalling about 615 children's sleepwear sets sold online from October to November 2021 because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Children's Sleepwear Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22730·2022-02-17

    Lovevery Steel Drinking Cups With Handle Recalled for Choking Hazard

    Lovevery is recalling steel drinking cups with handles included in Inspector Play Kits because the handle can detach, posing a choking hazard to young children. About 169,000 units were sold online from July 2018 through July 2021.

    Product
    Steel drinking cups with handle
    Category
    Consumer Product
    Distribution
    Distributed nationwide