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.

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19926–19950 of 90011

  • SevereFDA (Food)·F-0738-2023·2023-04-26

    Sheila G's Gluten Free Reese's Pieces Brownie Brittle recalled for undeclared wheat

    Sheila G's Gluten Free Reese's Pieces Brownie Brittle (4 oz bags, UPC 711747 011562) is being recalled because the product may contain undeclared wheat despite its gluten-free label, creating a risk for consumers with celiac disease or wheat allergies.

    Product
    Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC 711747 011562)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0734-2023·2023-04-26

    Volupta Organic Black Chia Seeds Recalled for Salmonella

    NSI Group LLC is recalling 1,351 pouches of Volupta Organic Black Chia Seeds distributed to a Costco location in San Diego, CA, due to Salmonella detected in product testing.

    Product
    Volupta Organic Black Chia Seeds 64 oz. Best By: 10/31/2025 Stand up pouch. Product of Paraguay
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0739-2023·2023-04-26

    Food Recall: HyVee Hamburger Chili Macaroni Skillet Meal – Undeclared Milk

    HyVee Hamburger Chili Macaroni Skillet Meal (5.2oz) is recalled due to undeclared milk allergen. The product was voluntarily recalled by the manufacturer and is no longer in distribution.

    Product
    HyVee Hamburger Chili Macaroni Skillet Meal, 5.2oz retail carton. UPC: 0 75450-08552 5
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·23V295000·2023-04-26

    BMW iX and i4 vehicles recalled for battery monitoring circuit defect

    BMW is recalling certain 2022-2024 iX xDrive50 and 2023 i4 models due to improperly secured electrical connections in the battery monitoring circuit, which can cause engine stall and increase crash risk.

    Product
    BMW — BMW IX, I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0737-2023·2023-04-26

    Kagome Chuno Sauce recalled for undeclared soy allergen

    North American Food Dist. Co., Inc. is recalling Kagome Chuno Sauce 16.9 fl. oz bottles (UPC 4901306097519) due to undeclared soy. Approximately 125 bottles were distributed in CA, CO, and NV.

    Product
    Kagome Chuno Sauce 16.9 fl., oz plastic bottles
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0736-2023·2023-04-26

    Kagome Worchester Sauce Recalled for Undeclared Soy Allergen

    Kagome Worchester Sauce in 16.9 fl. oz plastic bottles is recalled because it contains soy that is not declared on the label, posing a risk to consumers with soy allergies.

    Product
    Kagome Worchester Sauce 16.9 fl., oz plastic bottles
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1357-2023·2023-04-26

    Shiley Adult Flexible Tracheostomy Tubes Recalled Due to Undersized Connectors

    Covidien is recalling Shiley Adult Flexible Tracheostomy Tubes due to undersized connectors that create loose connections with 15mm respiratory circuit components. Unsecure connections could cause respiratory failure, difficulty breathing, treatment delays, or serious injury.

    Product
    Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner Cannula (REF, Product Description): 10CN10H, 10.0MM SHILEY CUFFED TRACH CAN; 10CN10R, 10.0MM ADT FLEX TRACH W TG CUFF; 10UN10A, 10.0MM UNCUFF TRACH TUBE X1…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0745-2023·2023-04-26

    Wegmans Chopped Spinach Recalled for Possible Rodent Contamination

    Wegmans brand steam chopped spinach may be contaminated with rodent hair and parts. Affected packages distributed in New York should be discarded or returned.

    Product
    WEGMANS STEAM CHOPPED SPINACH 12/12OZ Poly steam bags
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1412-2023·2023-04-26

    Spinal fixation screws recalled for reduced titanium gripping strength

    Medtronic is recalling 90 INFINITY Multi-Axial Screws (Lot H5806345) due to incorrect titanium material that reduces screw head gripping strength. The defect affects 5 batches distributed in the US and Canada.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 26mm, REF 3604026; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0740-2023·2023-04-26

    Jalapeno cheese sticks recalled for plastic foreign material

    Gilman Cheese Corporation is recalling jalapeno cheese sticks due to potential plastic fragments. Consumers should stop eating and discard the affected product.

    Product
    0.6 oz. jalapeno cheese sticks. P.6LGSTICKJL. Cheese sticks are packed in clear plastic pouches with a nitrogen flush. Pouches contain about 150 sticks, with 2 pouches per case. Cases can weigh between 9 lbs. - 11 lbs.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1409-2023·2023-04-26

    Spinal implant screws recalled due to defective titanium material

    Medtronic is recalling 45 units of INFINITY Multi-Axial Screws (lot H5802983) worldwide because incorrect titanium was used, reducing the screw head's gripping strength. No illnesses or injuries have been reported.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 24mm, REF 3604024; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2023·2023-04-26

    INFINITY Multi-Axial Spinal Screws Recalled for Titanium Material Defect

    Medtronic is recalling INFINITY Multi-Axial Spinal Screws due to incorrect titanium material used in manufacturing, which reduces the gripping strength of the screw head. The affected screws are used for spinal fusion and stabilization.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 34mm, REF 3604034; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1395-2023·2023-04-26

    Instrument Kit Drill Guides Have Incorrect Depth Range

    GEO Instrument Kits for EPS Plates contain drill guides marked with an incorrect depth range (30mm-60mm instead of 10mm-40mm), which could affect surgical implant placement.

    Product
    GEO Instrument Kit for EPS Plate, REF: 70120001, part of the GEO FirstFUSE 1st MTP Joint Arthrodesis Plating System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1401-2023·2023-04-26

    Medacta interbody fusion plate device recalled for screw breakage

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR interbody fusion device because the small screw affixing the anti-backout plate may break, potentially compromising device integrity.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighNHTSA·23V299000·2023-04-26

    Multiple Freightliner and Western Star Trucks Recalled for Electronic Stability Control Defect

    Daimler Trucks is recalling certain 2020-2024 Freightliner and Western Star trucks with an electronic stability control system that may cause understeering, increasing crash risk. Free tire replacement is being offered.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CLASSIC CASCADIA, CASCADIA, BUSINESS CLASS M2, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1392-2023·2023-04-26

    BioFire FilmArray GI Panel Recalled for Potential False Negative Results

    BioFire Diagnostics is recalling FilmArray Gastrointestinal Panel test kits due to a manufacturing issue that may produce false negative results. Affected units may fail to detect gastrointestinal infections.

    Product
    FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems, REF: RFIT-ASY-0116, (30 pouches/kit)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0741-2023·2023-04-26

    Matiz Piparra Peppers Recalled Due to Glass Contamination

    Power Selles Imports is recalling Matiz Piparra Peppers due to glass contamination. A shard of glass was found in one jar. Consumers should not consume the affected product.

    Product
    Matiz Piparra Peppers are packaged in a clear glass jar, net wt. 4lb. (1.8kg), drained wt. 25oz (700g). Product is shelf stable. UPC 832924005768. Produced By Conservas Rubio - Navarra, Spain. Imported By Matiz A Culinary Collective Company Lynnwood, WA.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0748-2023·2023-04-26

    Trader Joe's Chickenless Crispy Tenders Recalled for Foreign Material Contamination

    Dr. Praeger's Sensible Foods is recalling Trader Joe's Chickenless Crispy Tenders due to potential fibrous contamination. Consumers should discard the product or return it to the retailer.

    Product
    Trader Joe's Chickenless Crispy Tenders Net Wt, 8.1 OZ (230g) UPC 0097 8996 Packaged in a plastic bag
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1400-2023·2023-04-26

    FDA Recalls MectaLIF ANTERIOR Spinal Fusion Device Due to Screw Breakage Risk

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR Lag Plate Flush H10 interbody fusion device due to a potential risk of screw breakage in the anti-backout plate. No injuries have been reported.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Drugs)·D-0536-2023·2023-04-26

    Verapamil Hydrochloride Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Amerisource Health Services LLC is recalling Verapamil Hydrochloride Extended-Release Tablets 180 mg due to failed dissolution specifications affecting lots 1008622 and 1010026 distributed nationwide.

    Product
    Verapamil Hydrochloride Extended-Release Tablets, USP, 180 mg, 100 Tablets (10 x 10) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-504-01; NDC Unit Dose: 60687-504-11, barcode (01) 003 60687 504 11 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V298000·2023-04-26

    2023 Kia Sportage and Related Vehicles Instrument Cluster Display Failure

    The instrument cluster display in certain 2023 Kia vehicles may fail to show any information when started, preventing drivers from viewing critical safety data like tire pressure and warning lights. Kia will update the software for free.

    Product
    KIA — KIA TELLURIDE, SOUL, SPORTAGE, NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0539-2023·2023-04-26

    Antipsychotic Drug Recalled for Failed Quality Control Test

    Ascend Laboratories is recalling 135 bottles of Aripiprazole 20 mg tablets nationwide due to failure of spectroscopic identification testing, indicating the product may not meet established quality standards.

    Product
    ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0735-2023·2023-04-26

    Tried and True Granola recalled for undeclared milk allergen

    Bakery Barn has recalled Tried and True Granola products due to undeclared milk allergen. The recall affects 690 units distributed to retailers in Ohio and Pennsylvania.

    Product
    Tried and True Granola Co. Naturally Sweetened Granola packaged in 20lb bulk plastic bags and 14oz plastic containers
    Category
    Food
    Distribution
    2 states