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 the agency’s own highest classification or reported deaths or serious injuries, 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.

Filters

Agency

Category

Minimum severity

Clear filters

26276–26300 of 90150

  • HighFDA (Devices)·Z-0756-2022·2022-03-23

    DREAMTOME medical device recall: sterility compromised by barrier breach

    Fifteen Boston Scientific DREAMTOME medical devices are being recalled due to a sterile barrier breach that compromises device sterility. The affected lot number 27802363 requires appropriate action.

    Product
    DREAMTOME 49-20MM/450CM Material Number: M00584020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0799-2022·2022-03-23

    Lumbar Puncture Trays Recalled for Manometer Leaking and Assembly Defects

    Bard Peripheral Vascular Inc. is recalling 2,880 Lumbar Puncture Drug Free Trays due to defects in the manometer component involving leaking and mating issues that could affect device function.

    Product
    LUMBAR PUNCTURE DRUG FREE TRAY 22G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0748-2022·2022-03-23

    Diagnostic ultrasound system ACUSON Juniper fails to save study clips

    The ACUSON Juniper ultrasound system's clip storage function fails when the disk is full, potentially delaying treatment during critical imaging procedures. Healthcare facilities using this system should contact Siemens for support.

    Product
    Diagnostic Ultrasound System, ACUSON Juniper, UDI: (01)04056869152059, Model: 11335791, Rx, CE Ultrasound imaging system intended for the following applications: Vascular, Abdominal, Neonatal, Echocardiographical, Pediatric, Small Parts, Musculoskeletal, Obstetrical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V174000·2022-03-23

    2022 Alliance RV Valor Travel Trailers Recalled for Electrical Fire Hazard

    Alliance RV is recalling certain 2022 Valor, Paradigm, and Avenue travel trailers due to faulty power inlet bolts that can cause loose wiring and electrical fire risk. Dealers will replace the power inlet free of charge.

    Product
    ALLIANCE RV — ALLIANCE RV PARADIGM, AVENUE, VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0759-2022·2022-03-23

    Boston Scientific HYDRATOME RX Device Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling 7,695 units of HYDRATOME RX devices worldwide due to compromised sterility from a sterile barrier breach. Affected devices may pose a risk of infection.

    Product
    HYDRATOME RX 44-20MM/260CM Material Number: M00583040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0794-2022·2022-03-23

    FDA Recalls SAFE-T PLUS Lumbar Puncture Trays for Device Malfunction

    Bard Peripheral Vascular is recalling 49,760 SAFE-T PLUS lumbar puncture trays for adults due to manometer leaking and mating issues. Healthcare providers should discontinue use and contact the manufacturer.

    Product
    SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0796-2022·2022-03-23

    Lumbar Puncture Tray Recalled for Manometer Leaking and Connection Issues

    Bard Peripheral Vascular is recalling 29,870 lumbar puncture trays due to manometer failure that causes leaking and improper connections. The defect could compromise device function during lumbar puncture procedures.

    Product
    LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0874-2022·2022-03-23

    Bob Evan's Mashed Potatoes Recalled for Undeclared Wheat Allergen

    Bob Evan's Sour Cream & Chive Mashed Potatoes recalled due to incorrect packaging that failed to declare wheat allergen. Consumers with wheat allergies should not consume this product.

    Product
    Bob Evan's Sour Cream & Chive Mashed Potatoes 24oz plastic trays with clear film and sleeve over wrap sold as singles to consumers
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0889-2022·2022-03-23

    Basil Pesto Sauce Recalled Due to Plastic Contamination

    RMJV LP's First Street brand basil pesto sauce is recalled because hard plastic pieces were found in the product during manufacturing, traced to supplier ice.

    Product
    BASIL PESTO SAUCE FIRST STREET 6/8 OZ UPC: 0 41512 15550 5 Perishable. Keep refrigerated. Distributed by Amerifoods Trading Co. Los Angeles, CA 90051
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-0782-2022·2022-03-23

    LINQ II Insertable Cardiac Monitor Recalled for Moisture Ingress

    Medtronic is recalling 8 LINQ II Insertable Cardiac Monitors due to moisture ingress susceptibility that may cause loss of functionality. Affected devices were distributed in the US (NJ, NY, PA, VA) and Italy.

    Product
    LINQ II Insertable Cardiac Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0749-2022·2022-03-23

    Abbott Alinity s System software error affects diagnostic analyzer wash cycle

    Abbott Laboratories is recalling 306 units of Alinity s System software version 2.8.0 due to a software error causing insufficient wash buffer volume, which could affect diagnostic test accuracy.

    Product
    Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended for In Vitro diagnostic use only. The Alinity s System is a highthroughput, fully automated immunoassay analyzer designed to determine the presence of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0867-2022·2022-03-23

    Swanson Ultra Vitamin B12 Recalled for Potential Metal Shavings

    Swanson Health Products is recalling Swanson Ultra Vitamin B12 Methylcobalamin supplements due to potential metal shavings in the product. The contamination poses a choking and injury risk.

    Product
    Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per container, Item Code SWU122, UPC 87614-02122. Distributed by Swanson Health Products Fargo, ND 58104. 60 cc green PETE plastic bottle with black 33 induction seal cap
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0885-2022·2022-03-23

    Stutzman Farms Organic Einkorn Flour Recalled for Undeclared Wheat Allergen

    Stutzman Farms is recalling Organic All Purpose Einkorn Flour sold in bulk due to undeclared wheat allergen. The product was distributed across seven Midwest states.

    Product
    Stutzman Farms Organic All Purpose Einkorn Flour sold in bulk
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0887-2022·2022-03-23

    Fresh Creative Foods Thai Peanut Dressing Recalled for Plastic Contamination

    Fresh Creative Foods is recalling Thai Peanut Dressing due to the presence of hard plastic pieces potentially found in the product. The plastic originated from ice used during manufacturing.

    Product
    Fresh Creative Foods THAI PEANUT DRESSING R&G 80/2.5 OZ UPC: 10013454378387 Item # 402464 Perishable/Keep refrigerated
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-0764-2022·2022-03-23

    Medical device sterile barrier breach in Boston Scientific HYDRATOME RX

    Boston Scientific is recalling HYDRATOME RX 49-30MM/260CM devices worldwide because sterile barriers are compromised. The manufacturing defect affects device sterility.

    Product
    HYDRATOME RX 49-30MM/260CM Material Number: M00583010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0753-2022·2022-03-23

    Boston Scientific DREAMTOME device recalled due to sterile barrier breach

    Boston Scientific is recalling 12,067 DREAMTOME devices worldwide due to compromised sterility from a sterile barrier breach. The affected units may not be properly protected from contamination.

    Product
    DREAMTOME 44-30MM/260CM Material Number: M00584050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0767-2022·2022-03-23

    Boston Scientific Medical Device Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling 3,330 units of JAGTOME REVOLUTION RX devices due to a sterile barrier breach that compromises device sterility. The devices were distributed worldwide.

    Product
    JAGTOME REVOLUTION RX 39-30-260-025 Material Number: M00584260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0898-2022·2022-03-23

    Taiyaki Variety Pack recalled due to undeclared hazelnut allergen

    FDMR, Inc. (Suji's Korean Cuisine) is recalling Taiyaki Variety Pack because hazelnuts are listed in the ingredient statement but not in the allergen "Contains" statement, posing a risk to consumers with hazelnut allergies.

    Product
    Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container. Item Number 1598329, UPC: 8 50013 07258 3 Three flavors: Chocolate Cream, Vanilla Custard and Red Bean & Cinnamon. Manufactured for Suji's Korean…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2022·2022-03-23

    Sterile barrier breach recalled in Boston Scientific HYDRATOME RX catheters

    Boston Scientific is recalling HYDRATOME RX catheters due to sterile barrier compromise. The 112 affected units worldwide may pose infection risk if used.

    Product
    HYDRATOME RX 49-20MM/260CM Material Number: M00583000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0773-2022·2022-03-23

    Medical Device Sterility Compromise Recall by Boston Scientific

    Boston Scientific has recalled 3,578 units of the JAGTOME RX medical device due to sterility compromise from a barrier breach. Affected units were distributed worldwide.

    Product
    JAGTOME RX 44-20-260-035 Material Number: M00573040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0894-2022·2022-03-23

    Fresh Creative Foods Couscous Kit Recalled for Plastic Contamination

    Fresh Creative Foods has recalled its Autumn Couscous with Butternut Squash Kit due to hard plastic pieces found in the product from contaminated ice. No injuries have been reported.

    Product
    Fresh Creative Foods AUTUMN COUSCOUS W/ BUTTERNUT SQUASH KIT V 2/3.1875 LB UPC: 1001345432377 Item # 406627 Perishable/Keep refrigerated Kit Components: 2/2.75 lb. tubs of autumn couscous salad, 2/4 oz. bags of pecan cranberry blend, 1/6 oz. bags of product kit., distributed…
    Category
    Food
    Distribution
    20 states
  • HighNHTSA·22V175000·2022-03-23

    Brake pressure switch corrosion in Arcimoto motorcycles may cause constant brake lights

    Arcimoto Inc. is recalling certain 2019-2022 motorcycles because the brake pressure switch may corrode when exposed to salt and de-icer chemicals. Corroded switches cause brake lights to illuminate constantly, confusing other drivers and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV, ROADSTER, RAPID RESPONDER, DELIVERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0786-2022·2022-03-23

    Wright Medical ORTHOLOC Surgical Screw Recalled for Incorrect Component Packaging

    Wright Medical Technology's ORTHOLOC Non-Locking Screw was recalled due to a packaging error in lot #73967511638696, where locking screws were mistakenly packaged instead. The affected product was distributed to France.

    Product
    Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0761-2022·2022-03-23

    Boston Scientific Hydratome RX Devices Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling Hydratome RX 44-30MM/260CM devices due to a sterile barrier breach that could compromise device sterility. The recall affects 3,371 units distributed worldwide.

    Product
    HYDRATOME RX 44-30MM/260CM Material Number: M00583050
    Category
    Medical Device
    Distribution
    Distributed nationwide