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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19576–19600 of 27461

  • HighFDA (Devices)·Z-1046-2023·2023-02-08

    Medline UNITE Foot & Ankle Screw Recalled for Intra-Operative Failure

    Medline Industries is recalling 420 units of UNITE FOOT & ANKLE Screws nationwide due to observed intra-operative screw failure when used with specific drill bit sizes. The failure occurs due to excessive torque during surgical insertion.

    Product
    MEDLINE UNITE FOOT & ANKLE Screw, Polyaxial Locking, Mini T8 (2.0x8mm), REF MMSL2008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2023·2023-02-08

    Non-sterile procedural trays risk sterile packaging breach

    Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.

    Product
    Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0339-2023·2023-02-08

    Daim Swedish Almond Cake Recalled for Metal Contamination

    Almondy AB is recalling Daim Swedish almond cake (NET WT 14.1oz) due to discovery of a metal object in the product. Consumers should not eat affected cakes.

    Product
    Daim, Swedish almond cake with chocolate and crunchy caramel, Baked by Almondy, NET WT 14.1oz (400g)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1031-2023·2023-02-08

    Procedural trays recalled for potential sterile packaging breach

    Medline Industries recalls non-sterile procedural trays (LAPAROTOMY CDS) because sterile blades within the kits may puncture the outer foil packaging, compromising sterility.

    Product
    Non-sterile procedural trays labeled as LAPAROTOMY CDS, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23115·2023-02-08

    Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk

    Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.

    Product
    Fabuloso Multi-Purpose Cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1043-2023·2023-02-08

    Biomet Vanguard Knee Implant Components Recalled for Incorrect Labeling

    Biomet, Inc. is recalling specific Vanguard Knee System prosthetic components that are incorrectly labeled with wrong sizes and sides. This labeling error could result in incorrect implant placement during knee replacement surgery.

    Product
    (1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement prostheses. Item Number: 183122 EXPANDED RECALL: (2) Vanguard Knee System PS Open Box Femoral; Left; 60 mm. Item Number: 183124 (3) Vanguard Knee System PS Open Box Femoral; Left;
    Category
    Medical Device
    Distribution
    6 states
  • HighNHTSA·23V049000·2023-02-03

    Winnebago motorhome cooktops recalled for potential gas leak and fire risk

    Winnebago is recalling certain Travato, Solis, and Ekko motorhomes with Suburban cooktops that may develop gas leaks due to fractured burner tubes. In the presence of an ignition source, a leak poses a fire risk.

    Product
    WINNEBAGO — 2022 WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V051000·2023-02-03

    BMW S 1000 XR and R motorcycles recall for deactivated safety feature

    BMW is recalling 2020-2023 S 1000XR and 2022-2023 S 1000R motorcycles because a software update may have deactivated the front wheel lift-off assistant feature without notifying riders, increasing the risk of unexpected handling and loss of control.

    Product
    BMW — 2021 BMW S 1000 XR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V044000·2023-02-02

    Land Rover vehicles recalled for engine oil leak fire risk

    Jaguar Land Rover is recalling certain 2019-2023 Land Rover vehicles because the engine cam carrier oil channel may become blocked, causing an oil leak that could increase fire risk. No injuries have been reported.

    Product
    LAND ROVER — 2023 LAND ROVER DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V041000·2023-02-02

    2021 Toyota RAV4 Prime Engine Stall in Cold Weather Driving

    Toyota is recalling certain 2021 RAV4 Prime vehicles due to a software defect that may cause engine stall during cold-weather driving. Dealers will provide a free software update.

    Product
    TOYOTA — 2021 TOYOTA RAV4 PRIME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23111·2023-02-02

    Children's Robes Recalled for Flammability Standard Violation and Burn Hazard

    Betusline Official Apparel children's robes fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. About 350 units sold on Amazon.com from January through April 2022 are affected.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23110·2023-02-02

    Children's Robes Recalled for Flammability Standards Violation

    About 2,000 children's polyester robes imported by BTPEIHTD and sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop use immediately and contact the importer for a refund.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V046000·2023-02-02

    2020 Honda Fit rearview camera may not display on startup

    The rearview camera display may not activate when a 2020 Honda Fit is started with a key due to a display power circuit design error, reducing rear visibility and increasing crash risk. Dealers will provide a free software fix.

    Product
    HONDA — 2020 HONDA FIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23113·2023-02-02

    Children's Robes Recalled for Flammability Standards Violation and Burn Hazard

    About 3,000 SGMWVB brand children's robes sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk. Consumers should immediately stop using them and contact the manufacturer for a refund.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V048000·2023-02-02

    Incorrect defroster instructions in Nissan LEAF owner's manuals increase crash risk

    Nissan is recalling 2018-2023 LEAF vehicles because the Owner's Manual has incorrect defroster operation instructions, which may reduce visibility and increase crash risk. Nissan will mail updated instructions at no charge.

    Product
    NISSAN — 2021 NISSAN LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V043000·2023-02-02

    2023 GMC Acadia: Right-front half-shaft separation from transmission risk

    General Motors is recalling certain 2023 GMC Acadia vehicles because right-front half-shaft assemblies may separate from the transmission, potentially causing loss of drive power or vehicle rollaway and increasing crash risk.

    Product
    GMC — 2023 GMC ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23112·2023-02-02

    Children's Robes Recalled for Flammability Standards Violation

    ChildLikeMe children's robes sold on Amazon from January through April 2022 fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop use immediately and contact the importer for a refund.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V045000·2023-02-02

    2023 Jaguar F-Pace Engine Oil Leak Poses Fire Risk

    Jaguar is recalling 2023 F-Pace vehicles because the engine cam carrier oil channel may become blocked, causing an oil leak that could increase the risk of fire. Dealers will inspect and replace the affected engine components at no cost.

    Product
    JAGUAR — 2023 JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0184-2023·2023-02-01

    Vancomycin Hydrochloride Injection Recalled for Glass Particulate Matter

    Pfizer recalls approximately 89,700 vials of Vancomycin Hydrochloride for Injection due to glass particulate matter contamination. The recalled product (Lot 33045BA) was distributed across the USA and Puerto Rico.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0180-2023·2023-02-01

    Epinephrine API Recalled for Discoloration and Reduced Efficacy

    Spectrum Laboratory Products recalls Epinephrine (L-Adrenaline) USP in multiple lot sizes due to discoloration that could reduce the product's effectiveness. The recall affects shipments distributed nationwide in the USA, Puerto Rico, and Canada.

    Product
    Epinephrine (L-Adrenaline), USP, CAS 51-43-4, Packaged in amber glass bottles in a vacuum sealed pouch as (a)100 G; (b)1 G, (c) 25 G, (d) 5 G; Rx only. Repackaged by Spectrum Chemical Mfg. Corp. Gardena, CA 90248; New Brunswick, NJ 08901.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0960-2023·2023-02-01

    Getinge Flow-c Anesthesia System Software Bug May Prevent Ventilation

    The Getinge Flow-c Anesthesia System contains a software bug that can prevent pressure buildup and ventilation delivery. Under certain conditions, oxygen delivery may decrease, which may lead to hypoventilation and hypoxia.

    Product
    Getinge Flow-c Anesthesia System, Part No. 6887700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0181-2023·2023-02-01

    Advil Ibuprofen Tablets Recalled for Illegible Labels

    Glaxosmithkline Consumer Healthcare is recalling Advil ibuprofen 200 mg tablets because adhesive migrated onto labels, causing them to tear when peeled. This affects 321,246 tablets distributed nationwide.

    Product
    Advil (ibuprofen) Tablets, 200 mg, packaged as a) 360-count bottles (UPC 3 0573 0154 60 4), and b) 200-count bottles (UPC 3 0573 0154 21 5), Pfizer, Madison, NJ 07940
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0182-2023·2023-02-01

    Advil Liqui Gels Recalled Due to Illegible Labeling Defect

    Advil Liqui Gels (200mg ibuprofen capsules) are being recalled nationwide because adhesive on the packaging migrated onto the label, causing it to tear and become illegible when peeled back.

    Product
    Advil Liqui Gels, Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Distributed by: Pfizer, Madison, NJ 07940, UPC 3 0573 0169 49 3
    Category
    Drug
    Distribution
    Distributed nationwide