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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23351–23375 of 26062

  • HighFDA (Food)·F-0314-2022·2021-12-29

    Favorite Day Bakery Frosted Sugar Cookies Recalled for Potential Metal

    GIVE AND GO is recalling Favorite Day Bakery Frosted Sugar Cookies (13.5 oz., UPC 0 85239 41050 9) distributed nationwide due to potential metal contamination in the product.

    Product
    Favorite Day Bakery Frosted Sugar Cookies 13.5 oz. UPC 0 85239 41050 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0416-2022·2021-12-29

    Philips Allura Xper FD Ceiling Monitors Risk Falling Due to Loose Screws

    Set screws on ceiling-mounted extra monitors can loosen, causing monitors to fall and potentially injure patients, staff, or service technicians.

    Product
    Philips Allura Xper FD series with Software Version Number: 2.1.x- intended for Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. Model Number: 722005, 722006, 722008, 722010, 722012, 722013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0417-2022·2021-12-29

    Surgical Navigation Tracker Subject to Weld Failure and Navigation Inaccuracy

    A surgical navigation tracker used in neurosurgery may experience weld failure, leading to navigation inaccuracy, prolonged procedure time, and potential tissue injury. 98 affected units were distributed across US and international healthcare facilities.

    Product
    Stealth Autoguide Tracker, Model: 28248, which is an instrument in the Stealth Autoguide Basic Instrument Kit, Mode: 9736188, and the Bundle Autoguide Reg Kit.
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Food)·F-0289-2022·2021-12-29

    Kimberley's Bakeshoppe vanilla cupcakes recalled for potential metal

    GIVE AND GO is recalling Kimberley's Bakeshoppe vanilla cupcakes (11.2 oz.) nationwide due to the potential for metal in the product.

    Product
    Kimberley's Bakeshoppe vanilla cupcakes 11.2 oz. UPC 7 70981 31213 2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0407-2022·2021-12-29

    Cataract Surgery Kits Recalled for Compromised Sterile Packaging

    Beaver Visitec is recalling Malosa Core Phaco Pack 1 cataract surgery kits (Part Number: MMK833/2) because packaging may have small holes that compromise product sterility. The recall affects 120 units distributed across nine states.

    Product
    Malosa Core Phaco Pack 1-Medical Cataract Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK833/2
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0399-2022·2021-12-29

    Cholesterol Reagent Recalled for Calibration Failures and Erroneous Results

    Beckman Coulter is recalling 1,433 units of a cholesterol reagent that may fail calibration and produce erroneous low test results. Affected units were distributed nationwide and internationally.

    Product
    SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0287-2022·2021-12-29

    Give and Go Two-Bite Cupcakes Recalled for Potential Metal Contamination

    Give and Go is recalling two-bite vanilla and chocolate cupcakes nationwide due to the potential for metal in the product. Consumers should not eat the affected cupcakes and should return them to the place of purchase.

    Product
    two-bite vanilla & chocolate cupcakes 10 oz. UPC 7 70981 03127 9 20 oz. UPC 7 70981 03104 0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0291-2022·2021-12-29

    Rompe Pecho Cough Syrup Recalled for Microbial Contamination

    Efficient Laboratories, Inc. is recalling Rompe Pecho DM cough syrup (6 fl oz bottles) due to microbial contamination of the non-sterile product. The recall affects 27,206 bottles distributed nationwide.

    Product
    ROMPE PECHO — ROMPE PECHO (DEXTROMETHORPHAN HBR, GUAIFENESIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0348-2022·2021-12-29

    Twin Brook Creamery Pasteurized Milk Recalled for Inhibitory Substance

    Twin Brook Creamery brand pasteurized 1% milk in 64 oz and 32 oz glass bottles is being recalled because an inhibitory substance was detected. Fishtrap Dairy LLC is asking consumers not to consume the product.

    Product
    Twin Brook Creamery brand, Pasteurized 1% Milk, Vit D3 Vit A Palmitate, 100% Jersey Milk, packaged in 64 oz glass bottle with a green cap, Refrigerated, UPC8 97605 00102 6. Twin Brook Creamery brand, Pasteurized 1% Milk, Vit D3 Vit A Palmitate, 100% Jersey Milk, packaged in
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0409-2022·2021-12-29

    Malosa Core SMILE Pack Medical Refractive Kit Recalled for Packaging Defect

    Beaver Visitec International is recalling the Malosa Core SMILE Pack 1-Medical Refractive Kit because packaging may contain small holes that compromise sterility. The recall affects 680 units distributed in nine states.

    Product
    Malosa Core SMILE Pack 1-Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK884
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0300-2022·2021-12-29

    Carrot Cake Cupcakes Recalled for Potential Metal Contamination

    GIVE AND GO is recalling two carrot cake cupcake products nationwide due to the potential presence of metal in the product. Consumers should not consume affected lots and should contact the manufacturer or return the product to the place of purchase.

    Product
    two-bite carrot cake cupcakes 10 oz. UPC 7 70981 05525 1 Kimberley's bakeshoppe carrot cake filled gourmet cupcakes 11.5 oz. UPC 7 70981 31026 8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00K000·2021-12-28

    2022 Hyundai Santa Fe instrument cluster display may invert upon startup

    Hyundai is recalling certain 2022 Santa Fe PHEV and HEV vehicles because the instrument cluster display may invert upon startup, making it illegible and preventing drivers from seeing speed and safety warnings.

    Product
    HYUNDAI — 2022 HYUNDAI SANTA FE PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22714·2021-12-23

    Polaris RZR and GENERAL Recreational Off-Road Vehicles Steering Wheel Separation Recall

    Polaris is recalling about 8,800 RZR and GENERAL recreational off-road vehicles because the steering wheel can separate, causing loss of control and crash risk. Polaris has received 33 reports of broken or cracked steering wheel spokes, including five rollovers and two injuries.

    Product
    Polaris RZR and GENERAL Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E103000·2021-12-23

    Toyota power steering gear assembly recalled for oil leak risk

    Toyota is recalling power steering gear assemblies for certain Tundra and Sequoia models from 2007-2022. The components may be incorrectly manufactured, causing oil leaks that could result in sudden loss of power steering assist and increased crash risk.

    Product
    TOYOTA — 2007 TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00H000·2021-12-23

    Freightliner Custom Chassis recreational vehicles electrical lighting system failure

    Daimler Trucks North America is recalling Freightliner Custom Chassis recreational vehicles with defective power distribution modules that may disable brake lights, turn signals, and rear marker lights, reducing visibility and increasing crash risk.

    Product
    FCCC — 2016 FCCC XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22037·2021-12-22

    Royal Sovereign Portable Air Conditioners Recalled for Fire and Burn Hazards

    Royal Sovereign International is recalling about 33,570 portable air conditioners due to a faulty drain motor that can ignite the plastic enclosure, causing fires and burns. One death from smoke inhalation has been reported, along with 11 incidents of fires or smoking and over $1 million in property damage.

    Product
    Royal Sovereign/Royal Centurian portable air conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22039·2021-12-22

    Essential Medical Supply Endurance Hand Bed Rails Due to Entrapment and Asphyxiation

    Essential Medical Supply is recalling approximately 272,000 Endurance Hand Bed Rails because users can become entrapped within the rail or between the rail and mattress, posing a risk of asphyxiation. One death has been reported.

    Product
    Endurance® Hand Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·22036·2021-12-22

    Angel Line Bunk Beds with Angled Ladders Recalled for Entrapment and Strangulation Risk

    Longwood Forest is recalling Angel Line bunk beds with angled ladders because the metal hook fastening the ladder can detach or move, creating gaps that pose serious entrapment and strangulation hazards. A 2-year-old child died in May 2018 when found unresponsive in a bunk bed ladder gap.

    Product
    Angel Line Bunk Beds with angled ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22040·2021-12-22

    Carex Adult Portable Bed Rails Recalled After Three Deaths

    Compass Health Brands is recalling Carex Brand Adult Portable Bed Rails due to entrapment and asphyxiation hazards. Three deaths have been reported when users became trapped within the rails or between the rail and mattress.

    Product
    Carex Brand Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0322-2022·2021-12-22

    Country Time Lemonade Drink Mix Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Country Time Lemonade drink mix powder in five sizes due to potential contamination with glass and metal fragments. The recall affects approximately 289,221 cases distributed nationwide and internationally.

    Product
    Country Time Lemonade drink mix powder 19 oz. UPC 043000951170 29 oz. UPC 043000951194 63 oz. UPC 043000082195 82.5 oz. UPC 043000928608 116 oz. UPC 043000075388
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0358-2022·2021-12-22

    Livia One Organic Daily Topical Spray Probiotics recalled for Pseudomonas contamination

    Livia Global is recalling Livia One Organic Daily Topical Spray Probiotics because the product may be contaminated with Pseudomonas aeruginosa, a bacterium that can cause infection.

    Product
    Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: Spray affected area 2-5 times daily as needed. Ingredients: Proprietary probiotic blend in an enzyme enriched substrate: Lactobacillus-Acidophilus, L. Rhamn
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0280-2022·2021-12-22

    Lidocaine Topical Solution Recalled for Superpotency

    Teligent Pharma, Inc. is recalling Lidocaine Hydrochloride Topical Solution USP 4% nationwide due to the drug being superpotent. Affected lots are 13262 (Exp. 03/2022) and 14217 (Exp. 08/2022).

    Product
    Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena, NJ 08310, NDC 52565-009-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·22034·2021-12-22

    Hang-on Treestands Recalled Due to Cable Failure and Fall Hazard

    Big Game Treestands' 2021 The Captain model (batch 2M-0121) is recalled because plastic-coated cable crimps can slip during use, releasing the standing platform and causing falls. Two injuries have been reported from ten documented incidents.

    Product
    The Captain Hang-on Treestands (2021 Batch #2M-0121)
    Category
    Consumer Product
    Distribution
    Distributed nationwide