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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18501–18525 of 27457

  • HighFDA (Devices)·Z-1278-2023·2023-03-29

    Cardiosave IABP Safety Disk Model 0202-00-0140 Recalled for Performance Defect

    Datascope Corp. is recalling 669 Cardiosave IABP Safety Disks due to a performance defect that may reduce balloon inflation during cardiac support therapy. The affected devices may not provide adequate augmentation to patients requiring mechanical circulatory support.

    Product
    Cardiosave Intra-Aortic Balloon Pump (IABP) Safety Disk, Model Number 0202-00-0140
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·23V214000·2023-03-29

    2022 Volkswagen Taos Fuel Pump May Cause Engine Stall

    Volkswagen is recalling certain 2022 Taos vehicles because the fuel delivery pump may break and cause a sudden engine stall, increasing the risk of a crash.

    Product
    VOLKSWAGEN — 2022 VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1279-2023·2023-03-29

    Cardiosave IABP Pneumatic Interface Module Recalled for Performance Issue

    Datascope Corp. recalls the Cardiosave IABP Pneumatic Interface Module due to a Safety Disk performance issue that may reduce balloon inflation. Ten specific units with identified serial numbers are affected.

    Product
    Cardiosave Intra-Aortic Balloon Pump (IABP) Pneumatic Interface Module (PIM) , Model Number 0997-00-1178
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0642-2023·2023-03-29

    Kurata Menzo Ramen Recalled for Undeclared Coconut Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling Kurata Menzo Meatfree Tonkotsu Ramen Dry due to undeclared coconut on the label. Consumers with coconut allergies who consume this product may experience allergic reactions.

    Product
    Kurata Menzo Meatfree Tonkotsu Ramen Dry 2P 238.8g UPC: 4906436004932 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0634-2023·2023-03-29

    Coffee Candy Recalled for Undeclared Coconut Allergen

    Kanro Non sugar coffee candy is recalled because coconut was not declared on the label, posing a risk to consumers with coconut allergies.

    Product
    Kanro Non sugar coffee candy 40g UPC: 4901351013137 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0648-2023·2023-03-29

    Kirkland Signature Colombian cold brew coffee recalled for metal contamination

    Berner Foods Inc. is recalling Kirkland Signature Colombian Cold Brew Coffee due to metal contamination in 231,071 cases distributed across 13 states. Consumers should stop using affected products.

    Product
    Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-0699-2023·2023-03-29

    Sprouts Farmers Market Saltine Crackers recalled for potential peanut contamination

    Sprouts Farmers Market is recalling Saltine Crackers Sea Salt Tops due to potential peanut contamination. Approximately 1,050 cases were distributed in Arizona, California, and Georgia.

    Product
    Sprouts Farmers Market Saltine Crackers Sea Salt Tops NET WT 16 OZ (1 LB) 454g UPC 646670310164 packaged in slug wrapper in a cardboard carton, 12 packages per case
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0636-2023·2023-03-29

    Soft rice crackers recalled for undeclared coconut allergen

    DAISO CALIFORNIA WAREHOUSE is recalling 150YEN HIZATSUKI Soft rice crackers because the product contains coconut that was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    150YEN HIZATSUKI Soft rice crackers sea lettuce soy sauce flavor UPC: 4902445210500 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0646-2023·2023-03-29

    BODYARMOR SportWater recalled for potential plastic pieces

    BA Sports Nutrition is recalling BODYARMOR SportWater due to potential plastic pieces in the product. The recall affects approximately 21 million bottles distributed across 11 states.

    Product
    BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR SportWater 15/1L Club
    Category
    Food
    Distribution
    11 states
  • HighFDA (Drugs)·D-0468-2023·2023-03-29

    Prescription Drug Recall: Jardiance Empagliflozin 25 mg Label Mix-Up

    Boehringer Ingelheim Pharmaceuticals is recalling Jardiance (Empagliflozin) 25 mg tablets due to a label mix-up affecting 69,375 bottles distributed nationwide.

    Product
    JARDIANCE — JARDIANCE (EMPAGLIFLOZIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1263-2023·2023-03-29

    Orthopedic Implant Recall: Excessive Radiation Exposure in Revision Tibial Insert

    DePuy Orthopaedics recalls 7 units of Attune Revision LPS Tibial Inserts (Part 151760118, Lot JP6452) distributed worldwide due to excessive gamma radiation during manufacturing. This overage may result in material property changes.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1265-2023·2023-03-29

    Attune Revision Limb Preservation System Tibial Insert Recalled for Over-Irradiation

    DePuy Orthopaedics is recalling 7 units of the Attune Revision Limb Preservation System Tibial Insert (Lot JP9022) that received higher than specified gamma radiation doses. The over-irradiation may cause changes to implant material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0649-2023·2023-03-29

    WHH A&D Calcium Milk Drink Recalled for Undeclared Milk Allergen

    WHH A&D Calcium Milk Drink recalled due to undeclared milk on the ingredient label. The recall affects 12,000 units distributed in California.

    Product
    WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles in 1 pack Made in China
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0644-2023·2023-03-29

    Onishi Foods Alpha Rice Recalled for Undeclared Coconut Allergen

    Onishi Foods Alpha Rice Matsutake Mushroom Rice is being recalled because the label does not declare coconut, a major allergen. The recall affects 733 units distributed in multiple US states and Canada.

    Product
    Onishi Foods Alpha Rice Matsutake Mushroom Rice 100g UPC: 4970088140331 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1267-2023·2023-03-29

    DePuy Attune Tibial Insert Recalled for Excessive Radiation Exposure

    DePuy Orthopaedics is recalling Attune Posterior tibial insert implants that received excessive gamma radiation during manufacturing, which may degrade the material properties of the knee replacement component.

    Product
    Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1280-2023·2023-03-29

    Wearable ECG smartwatch software bug eliminates physician review

    Withings Scan Monitor/ScanWatch (model hwa09) has a software defect preventing physicians from reviewing ECG recordings, which is critical to the device's FDA clearance requirement for physician-supervised use. Users should discontinue use until the defect is corrected.

    Product
    Scan Monitor/ScanWatch, model number hwa09 Wearable, Bluetooth-connected wrist watch that records heart activity (ECG) and oxygen saturation (SpO2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0641-2023·2023-03-29

    Igarashiseimen Kitakata Spicy Umakara Ramen Recalled for Undeclared Coconut Allergen

    Igarashiseimen Kitakata Spicy Umakara Ramen is being recalled because coconut allergen is not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Igarashiseimen Kitakata Spicy Umakara Ramen UPC: 4967448174211 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0472-2023·2023-03-29

    Daytrana methylphenidate patches recalled for defective delivery system

    Noven Pharmaceuticals is recalling Daytrana methylphenidate transdermal patches for a defective delivery system that fails to meet shear specifications. The recall affects specific lots distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2023·2023-03-29

    BD Pyxis Automated Medication Dispensing Systems Firmware Downgrade Recall

    CareFusion recalls 7,914 units of BD Pyxis automated medication dispensing systems after firmware was inadvertently downgraded during installation, potentially causing drawer failures and medication delivery delays.

    Product
    BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES Tower (Med ES Tower), REF: 352; all with BD Pyxis ES version 1.6.1 drawer firmware (version 1.10.2.5). Pyxis MedStation Enterprise Server (ES) System is an a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2023·2023-03-29

    Japanese Potato Yokan Candy Recalled for Undeclared Coconut

    Kinjo Seika Potato Yokan confection is being recalled because coconut, a major allergen, was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Kinjo Seika Potato Yokan 130g UPC: 4901324017056 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0626-2023·2023-03-29

    MEITO Alphabet Chocolate recalled for undeclared coconut allergen

    MEITO Alphabet Chocolate 50g packages sold in multiple U.S. states and Canada were distributed with undeclared coconut allergen. Consumers with coconut allergies should not consume this product.

    Product
    MEITO Alphabet Chocolate 50g 50g UPC: 4902757130909 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0627-2023·2023-03-29

    Alpha Rice Mushroom Rice Recalled for Undeclared Coconut Allergen

    Onishi Foods Alpha Rice Mushroom Rice is recalled due to undeclared coconut allergen on the label. Consumers with coconut allergies should not consume this product.

    Product
    Onishi Foods Alpha Rice Mushroom Rice 100g UPC: 4970088140546 Made in Japan
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1272-2023·2023-03-29

    Disposable Patient Circuit with Precision Flow System recalled for excessive condensation

    Vapotherm has recalled 5,869 Low Flow Disposable Patient Circuits for the Precision Flow System due to reports of excessive condensation that may lead to rainout.

    Product
    Low Flow Disposable Patient Circuit for the Precision Flow System, Product Code PF-DPC-LOW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V208000·2023-03-28

    Freightliner Cascadia and Western Star 49X hazard light malfunction recall

    Daimler Trucks North America is recalling 2020-2021 Freightliner Cascadia and Western Star 49X vehicles because hazard warning lights may flash improperly during Advanced Braking Assist events, potentially confusing other drivers and increasing crash risk.

    Product
    FREIGHTLINER — 2020 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V210000·2023-03-28

    2023 Genesis G90 seat belt pretensioners may explode during crashes

    Hyundai is recalling 575 units of the 2023 Genesis G90 because the seat belt pretensioners may explode in a crash. Metal fragments from the explosion may strike and injure vehicle occupants.

    Product
    GENESIS — 2023 GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide