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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13976–14000 of 89754

  • SevereFDA (Food)·F-1029-2024·2024-03-13

    Chicken Enchilada with Rice & Beans Recalled for Listeria Contamination

    The Fierro Group Inc. is recalling Chicken Enchilada with Rice & Beans products due to potential Listeria monocytogenes contamination in the Queso Fresno cheese. Affected products were distributed to supermarkets in Utah.

    Product
    Chicken Enchilada with Rice & Beans/Green 14 oz. packaged in a in a Deep Meal tray Plant Fiber - Film 800.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1028-2024·2024-03-13

    Cheese Enchiladas Recalled Due to Potential Listeria Monocytogenes Contamination

    The Fierro Group Inc. is recalling cheese enchiladas with green sauce due to potential Listeria monocytogenes contamination. Products were distributed to supermarkets in Utah.

    Product
    Cheese Enchiladas with Green sauce 4/pkg 14.5oz packaged in a in a Deep Meal tray Plant Fiber - Film 800.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1024-2024·2024-03-13

    Golden Owl Dried Mango Recall for Undeclared Sulfites

    Golden Owl Dried Mango (7 oz) is recalled due to undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    Golden Owl Dried Mango 7 oz (200g) UPC 816710-024461. Packaged in clear non-flex plastic jars. 24 jars per case.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1039-2024·2024-03-13

    Classic Castle Shredded Three Cheese Blend Recalled for Listeria Risk

    Classic Castle Brand Shredded Three Cheese Blend has been recalled due to potential contamination with Listeria monocytogenes. Consumers should not consume affected products.

    Product
    Classic Castle Brand Shredded Three Cheese Blend Net Wt. 20 Lbs, Net Wt. 5 lbs. Fontana, CA 92336 Plant #06-00333
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1053-2024·2024-03-13

    BANH PIA Pumpkin Pia Cake Recalled for Undeclared Egg Allergen

    BANH PIA Liu Sha Pumpkin Pia Cake is recalled because it contains egg that is not declared on the label. The recall affects 222,320 bags distributed across 31 US states and Canada. Consumers with egg allergies should not consume this product.

    Product
    BANH PIA Liu Sha Pumpkin Pia Cake, 480g
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1025-2024·2024-03-13

    Taylor Fresh Foods Marketside Salad Kit Recalled for Potential Listeria Contamination

    Taylor Fresh Foods is recalling Marketside Bacon Ranch Crunch Chopped Salad Kits due to potential Listeria monocytogenes contamination. Affected products with best-by dates on or before Feb 21, 2024 were distributed to 28 states.

    Product
    Marketside Bacon Ranch Crunch Chopped Salad Kit 12.76oz UPC 681131305440
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-1040-2024·2024-03-13

    Chick-fil-A Polynesian Sauce Cup recalled for undeclared wheat and soy allergens

    T Marzetti Co is recalling Chick-fil-A Polynesian Sauce Cups (28g single serve) due to undeclared wheat and soy allergens. The product was distributed across 11 U.S. states.

    Product
    Chick-fil-a Polynesian Sauce Cup: 28g single serve food service cup
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-1047-2024·2024-03-13

    FDA recalls Banh Pia Classic Hopia for undeclared egg allergen

    LQNN Inc. is recalling Banh Pia Classic Hopia because it contains undeclared egg allergen, which can cause serious allergic reactions. About 222,320 bags were distributed across 31 U.S. states and Canada.

    Product
    Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1030-2024·2024-03-13

    Chicken Enchilada Recall: Listeria Risk from Queso Fresno Cheese

    The Fierro Group Inc. (Rico Brands) is recalling Chicken Enchilada with Mole Rice & Beans due to potential Listeria monocytogenes contamination in the Queso Fresno cheese. Affected products were distributed to supermarkets in Utah.

    Product
    Chicken Enchilada with Mole Rice & Beans 14 oz. packaged in a in a Deep Meal tray with Plant Fiber - Film 800.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1052-2024·2024-03-13

    Vegetarian Pia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling Vegetarian Pia Cake Red Bean Durian products due to undeclared egg allergen. The recall affects 222,320 bags distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Red Bean Durian, 14oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-1187-2024·2024-03-13

    Avanos Medical recalls MIC gastric-jejunal feeding tubes with defective syringe

    Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits containing a sterile pre-filled syringe that was recalled by Nurse Assist. Approximately 53,126 units were distributed worldwide.

    Product
    MIC* Gastric-Jejunal Feeding Tube, Endoscopic/Radiologic Placement, GJ-Tube: a) MIC* Gastric-Jejunal Feeding Tube Kit - Endoscopic/Radiologic Placement - 16 Fr, Product Code 0250-16; b) MIC* Gastric-Jejunal Feeding Tube Kit - Endoscopic/Radiologic Placement - 16 Fr, Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1276-2024·2024-03-13

    ConvaTec Natura Stomahesive surgical ostomy system pouch-flange coupling mismatch

    ConvaTec Natura Stomahesive ostomy kits contain a 45mm flange but 57mm pouch, creating an incompatible coupling. The mismatch prevents the components from fitting together properly.

    Product
    ConvaTec Natura Stomahesive Post-Operative / Surgical Ostomy System, REF 416938, 1 3/4 in. 45mm, Sterile.
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-1022-2024·2024-03-13

    Frothy Monkey Ham & Cheese Croissant Recalled for Potential Metal Fragments

    Bakery by Frothy Monkey is recalling Ham & Cheese Croissants due to potential metal fragments in the product. Consumers should not consume affected units.

    Product
    Frothy Monkey - Ham & Cheese Croissant - packaged and sold individually
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1263-2024·2024-03-13

    Orthopedic knee implant recalled for potential sterile packaging breaches

    Howmedica Osteonics Corp. is recalling the NO 3 Triathlon TS Plus Tibial Insert due to potential breaches in the sterile packaging. The breaches could compromise product sterility and safety.

    Product
    NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·013-2024·2024-03-13

    Kroger Apple Walnut Chicken Salad Bowl Recalled for Undeclared Wheat

    Taylor Farms Pacific is recalling Kroger brand apple walnut with chicken salad bowls due to undeclared wheat allergen. No adverse reactions have been reported.

    Product
    Taylor Farm - Pacific — Taylor Farms Pacific Recalls Kroger Brand Ready-To-Eat Apple Walnut With Chicken Salad Bowl Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1225-2024·2024-03-13

    Laboratory analyzer software defect may cause erroneous patient test results

    A software defect in VITROS 4600 Chemistry Systems causes quality control baselines to not update when users change them, potentially causing erroneous patient results.

    Product
    VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440 (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1232-2024·2024-03-13

    Laboratory chemistry system software defect impairs quality control reporting

    A software defect in VITROS XT 3400 Chemistry Systems prevents quality control rules from properly reporting failures in test controls. This may result in erroneous patient test results being reported.

    Product
    VITROS XT 3400 Chemistry System, Catalog No. 6844458
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1230-2024·2024-03-13

    VITROS 4600 Chemistry System Software Defect Affects Quality Control Reporting

    A software defect in VITROS 4600 Chemistry Systems running software versions 3.8.0 or 3.8.1 prevents quality control rules from being flagged or reported correctly, potentially allowing erroneous patient results to be released.

    Product
    VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440 (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1234-2024·2024-03-13

    Titanium Hindfoot Arthrodesis Cannulated Nails Recalled Due to Sterilization Failure

    Synthes recalls 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails (5 units) due to failed sterilization. These surgical implants were distributed worldwide and pose infection risk if implanted.

    Product
    13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX, sterile -Intended to facilitate tibiotalocalcaneal arthrodesis to treat severe foot/ankle deformity, arthritis, instability, and skeletal defects after tumor resection. Part Number: 04.008.378S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2024·2024-03-13

    FUJIFILM Synapse PACS Software Produces Incorrect Breast Imaging Measurements

    FUJIFILM is recalling Synapse PACS Version 7.2.100 because the medical imaging software produces incorrect measurements when analyzing certain breast images. Affected healthcare facilities using this software version should verify measurement accuracy in their systems.

    Product
    Synapse PACS - Version 7.2.100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1240-2024·2024-03-13

    TFNA Femoral Nail Recalled Due to Sterility Confirmation Issue

    Synthes is recalling 11 TFNA Femoral Nails due to sterility failures. The affected units worldwide cannot be confirmed as sterilized and pose infection risks to patients.

    Product
    TFNA Femoral Nail 11mm, right, 130¿, L 235mm-Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.144S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1254-2024·2024-03-13

    Paragon 28 Phantom TTC Nail distributed prior to sterilization

    Paragon 28 is recalling Phantom TTC Nails distributed before sterilization. Non-sterile surgical devices pose a potential infection risk if implanted.

    Product
    Phantom TTC Nail, 10.0 X 200mm, Right
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1222-2024·2024-03-13

    VITROS XT7600 System Aspiration Risk During Sample Processing

    Ortho-Clinical Diagnostics is recalling the VITROS XT7600 Integrated System due to potential aspiration from unintended sample containers during processing, which may result in erroneous test results. The recall affects 1,720 units distributed worldwide.

    Product
    VITROS XT7600 Integrated System
    Category
    Medical Device
    Distribution
    Distributed nationwide