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

14351–14375 of 89769

  • HighFDA (Drugs)·D-0330-2024·2024-02-28

    Kroger Cherry Cough Drops recalled for potential glass and silicone contamination

    Bestco LLC is recalling Kroger Cherry Cough Drops due to potential glass and silicone particulates in the product. The recall affects product distributed nationwide.

    Product
    Kroger Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000064, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0912-2024·2024-02-28

    Country Corner Dairy White Colby Cheese Recalled for Improper Pasteurization

    Country Corner Dairy is recalling WHITE COLBY CHEESE products due to improper pasteurization. The recalled products were distributed to Maryland and Virginia.

    Product
    Fresh Local , Country Corner Dairy, WHITE COLBY CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0896-2024·2024-02-28

    Wheat Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling bleached wheat flour due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across six states.

    Product
    BLEACHED WHEAT FLOUR 5600352 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0889-2024·2024-02-28

    Bulk Baking Ingredient Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling SPECIAL CAKE 53869 bulk ingredient due to potential contamination with metal, wood, and other foreign material. Affected product was distributed in six states.

    Product
    SPECIAL CAKE 53869 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1146-2024·2024-02-28

    Henry Schein Criterion Level 3 Earloop Masks Recalled for Non-Validated Equipment

    AMD Medicom Inc. is recalling Henry Schein Criterion Level 3 Earloop Masks because they were produced on non-validated equipment not included in the initial product qualification.

    Product
    HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0340-2024·2024-02-28

    Prescription injection drug recalled due to temperature excursion during shipment

    Acthar Gel (repository corticotropin injection) is being recalled due to a temperature excursion during shipping from the manufacturer to distributor. Lot #1564-103 should not be dispensed to patients.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1171-2024·2024-02-28

    Cardiology imaging software may calculate heart chamber size incorrectly

    Synapse Cardiology PACS software versions 7.0–7.3.0 may calculate left ventricle mass incorrectly, potentially leading to misdiagnosis or wrong treatment plans. Thirteen units have been distributed in the US and Israel.

    Product
    Synapse Cardiology PACS V7.3.0, V7.2, V7.1, V7.0. A web-based application as the primary user interface for the processing of medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0900-2024·2024-02-28

    Bulk Animal Feed Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling non-human consumption feed products due to potential contamination with metal, wood, and gasket material. Approximately 2.6 million pounds were distributed across six states.

    Product
    NON-HUMAN CONSUMPTION delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0881-2024·2024-02-28

    Bulk animal feed product recalled for potential foreign material contamination

    Mennel Milling Company is recalling 2ND CLEAR 1051664, a bulk animal feed product, due to potential contamination with metal, wood, gasket material, and sifter balls. Affected products were distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2ND CLEAR 1051664 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1174-2024·2024-02-28

    Aquabiliti saline flush syringes recalled for potential sodium chloride content deficiency

    MRP, LLC is recalling AQUABILITI AQUASTAT saline flush syringes because they may fail to meet USP standards for sodium chloride content after 12 months.

    Product
    AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL in 12mL, REF 2T0807, intermediate cartons containing 100 syringes, shipping cases containing 400 syringes, Rx, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0326-2024·2024-02-28

    Fluticasone Propionate Nasal Spray Recalled for Potential Bacterial Contamination

    Apotex Corp. is recalling Fluticasone Propionate Nasal Spray (292,752 bottles nationwide) due to potential Burkholderia cepacia contamination from manufacturing deviations. No illnesses reported.

    Product
    FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0339-2024·2024-02-28

    Fosfomycin Tromethamine Granules Recalled for Out-of-Specification Organic Impurities

    Ascend Laboratories recalls 71,244 sachets of Fosfomycin Tromethamine for failing quality specifications due to organic impurities. Patients with affected lots should consult their healthcare provider.

    Product
    FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0893-2024·2024-02-28

    Bulk Product Recalled for Potential Metal, Wood, and Foreign Material Contamination

    Mennel Milling Company is recalling bulk product 2-00007-0000 due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2-00007-0000 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1150-2024·2024-02-28

    Epidural Tray Kits Recalled for Wrong Connector Type

    B. Braun Medical recalls 3,890 PERIFIX epidural trays nationwide due to filter straws with incompatible neuraxial connectors instead of standard Luer connectors.

    Product
    Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray (Kit) A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. It includes the pharmaceutical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0885-2024·2024-02-28

    Mennel Milling Company Recalls Dried Grain Product for Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of DRIED SOFT 75 ENR 134348 due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    DRIED SOFT 75 ENR 134348 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1151-2024·2024-02-28

    Philips Allura Xper X-ray systems disk bay component may malfunction

    Philips has recalled certain Allura Xper interventional X-ray systems because the disk bay component may fail, potentially preventing system operation and imaging procedures.

    Product
    Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1179-2024·2024-02-28

    Biliary Endoprosthesis Labeling Mismatch Risks Incorrect Device Placement

    W.L. Gore's GORE VIABIL Short Wire Biliary Endoprosthesis may be mislabeled regarding drainage holes, risking extended procedures, infections, and unplanned device removal in 24 units distributed in Georgia.

    Product
    GORE VIABIL Short Wire Biliary Endoprosthesis, Product labeled as (1) Catalog Number VSWVH1008, 10 mm x 8 cm; with holes; and (2) Catalog Number VSWVN1008, 10 mm x 8 cm; no holes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0914-2024·2024-02-28

    Country Corner Dairy Yellow Cheddar Cheese Recall Due to Improper Pasteurization

    Country Corner Dairy is recalling Yellow Cheddar Cheese due to lack of proper pasteurization. The product was distributed in Maryland and Virginia and may pose a food safety risk.

    Product
    Fresh Local , Country Corner Dairy, YELLOW CHEDDAR CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Color, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1149-2024·2024-02-28

    PERIFIX epidural kits recalled for incompatible filter straw connectors

    B. Braun PERIFIX epidural kits contain filter straws with Neuraxial connectors instead of Standard Luer Connections, preventing proper assembly of the kits.

    Product
    Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX FX 19 Ga. Springwound Closed Tip Catheter, 5 mL Glass Luer Lock LOR Tray (Kit)-A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1177-2024·2024-02-28

    Azurion 5 X-Ray System Generator May Fail Due to Circuit Short

    Philips Azurion 5 X-ray systems with Certeray generators may experience power loss due to a potential short circuit in the power inverter board, potentially delaying or interrupting medical procedures.

    Product
    Azurion 5 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722227 (2) 722228
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1144-2024·2024-02-28

    Philips Allura Xper Interventional X-ray System Display and Imaging Malfunction

    A framegrabber card malfunction in Philips Allura Xper interventional X-ray systems may cause display failures, preventing proper visualization of medical images and delaying procedures.

    Product
    Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1154-2024·2024-02-28

    X-Ray C-Arm System Internal Board Defect Causes Abnormal Images

    Canon Medical System X-ray C-arm systems may display abnormal images due to an internal board manufacturing defect, potentially preventing exam completion and requiring patients to be re-examined with alternative equipment.

    Product
    The device is an X-ray system that is capable of radiographic and fluoroscopic studies and is used in an interventional setting. The system consists of a C-arm which is equipped with an X-ray tube, beam limiter and X-ray receptor, X-ray controller, computers with system and…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0906-2024·2024-02-28

    Fortune cookies recalled for undeclared soy allergen

    Fortune cookies manufactured by New World Company are being recalled due to undeclared soy allergen. Consumers with soy allergies should not consume the product.

    Product
    Fortune cookies, individually wrapped in a 6lb case, 190 pcs / case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0897-2024·2024-02-28

    Pizza Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling pizza flour due to potential contamination with metal, wood, gasket material, and sifter balls. Approximately 2.6 million pounds were distributed across Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    PIZZA FLOUR EN MA BL delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1147-2024·2024-02-28

    Henry Schein Criterion Anti-Fog Earloop Masks Recalled for Equipment Validation Issue

    AMD Medicom Inc. is recalling Henry Schein Criterion Anti-Fog Earloop Masks Level 3 (Blue) because the masks were produced on non-validated equipment not included in the product qualification process.

    Product
    HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)
    Category
    Medical Device
    Distribution
    Distributed nationwide