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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14576–14600 of 31507

  • 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
    0 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
    0 states
  • 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
    0 states
  • SevereFDA (Food)·F-1048-2024·2024-03-13

    BANH PIA Hopia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling BANH PIA Hopia Cake Mungbean Durian due to undeclared egg allergen. The product was distributed to customers in 31 U.S. states and Canada.

    Product
    BANH PIA Hopia Cake Mungbean Durian, 9.7oz (275g)
    Category
    Food
    Distribution
    0 states
  • 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
    0 states
  • SevereFDA (Devices)·Z-1186-2024·2024-03-13

    MIC Gastric-Jejunal Feeding Tube Kits Recalled Over Defective Syringe

    Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits because they contain a sterile pre-filled syringe that was subsequently recalled by Nurse Assist. Approximately 10,808 units have been distributed worldwide.

    Product
    MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector - Endoscopic/Radiologic Placement - 16 Fr, Product Code 8250-16; b) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector - Endoscopic/Radiologic Pla
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1027-2024·2024-03-13

    Cheese Enchiladas Recalled for Potential Listeria Monocytogenes Contamination

    The Fierro Group Inc. is recalling Cheese Enchiladas with Red sauce due to potential contamination with Listeria monocytogenes. Products were distributed to supermarkets in Utah.

    Product
    Cheese Enchiladas with Red sauce 4/pkg 14.5oz packaged in a in a Deep Meal tray Plant Fiber - Film 800.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1046-2024·2024-03-13

    Vegetarian Pia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling approximately 222,320 bags of Vegetarian Pia Cake Black Sesame Durian due to undeclared egg. Consumers with egg allergies should not consume this product.

    Product
    Vegetarian Pia Cake Black Sesame Durian, 14oz (400g)
    Category
    Food
    Distribution
    0 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-1043-2024·2024-03-13

    Vegetarian Pia Cake Mung Bean Pumpkin Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Mung Bean Pumpkin because the product contains undeclared egg allergen. Consumers with egg allergies should not eat this product.

    Product
    Vegetarian Pia Cake Mung Bean Pumpkin, 14 oz (400g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1042-2024·2024-03-13

    BANH PIA Hopia Cake Recalled Due to Undeclared Egg Allergen

    LQNN Inc. is recalling BANH PIA Hopia Cake due to undeclared egg allergen. Approximately 222,320 bags were distributed to 31 U.S. states and Canada.

    Product
    BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)
    Category
    Food
    Distribution
    0 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
    0 states
  • 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 (Devices)·Z-1246-2024·2024-03-13

    Aesculap Disposable Trocars with Dilating Pins Recalled for Packaging Damage

    Aesculap Inc is recalling disposable trocars with dilating pins due to potential sterile blister packaging damage that may compromise sterility. The affected product (code EK236SU) was distributed in the US and Canada.

    Product
    DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2024·2024-03-13

    Medical Device Imaging Software May Calculate Incorrect Breast Measurements

    Synapse PACS Version 7.1.000US may produce incorrect measurements when Secondary Capture 2D images lack pixel spacing information in the DICOM header. The affected software is installed in healthcare facilities worldwide, including the United States and Puerto Rico.

    Product
    Synapse PACS - Version 7.1.000US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1253-2024·2024-03-13

    Apollo Onyx Delivery Microcatheter recalled for incorrect indications for use

    Micro Therapeutics is recalling Apollo Onyx Delivery Microcatheter devices with incorrect indications for use. European-version devices were distributed in the U.S. across 29 states.

    Product
    The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the Onyx liquid embolic system (LES). The catheter has a semi-rigid proximal shaft and a highly flexible distal shaft to facilitate the advancement of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1224-2024·2024-03-13

    Medical Device: VITROS 3600 immunodiagnostic system software defect may produce incorrect results

    A software defect in the VITROS 3600 Immunodiagnostic System may cause quality control baseline statistics to fail to update properly, potentially resulting in erroneous patient test results.

    Product
    VITROS 3600 Immunodiagnostic System Catalog Nos. 6802783 (regular) and 6802914 (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1243-2024·2024-03-13

    Aesculap Disposable Trocar with Dilating Pin Recalled for Compromised Sterility

    Aesculap Inc is recalling Disposable Trocars with Dilating Pins (Product Code EK224SU) due to potentially damaged sterile blister packaging that may compromise sterility. Affected units were distributed in the US and Canada.

    Product
    DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1220-2024·2024-03-13

    VITROS 3600 Immunodiagnostic Systems May Cause Aspiration During Sample Processing

    The VITROS 3600 Immunodiagnostic System is being recalled due to potential aspiration of sample containers during laboratory processing, which may result in erroneous test results.

    Product
    VITROS 3600 Immunodiagnostic System (New and Refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1235-2024·2024-03-13

    Synthes 1.5MM Surgical Drill Bit Recalled Due to Sterilization Concerns

    Synthes has recalled 17 units of 1.5MM surgical drill bits worldwide because the products could not be confirmed as sterilized, posing an infection risk during orthopedic procedures.

    Product
    1.5MM Drill Bit/QC/85MM Sterile-surgical, orthopedic, pneumatic powered & accessory/attachment Part Number: 310.15S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1228-2024·2024-03-13

    Medical device software defect may cause incorrect laboratory test results

    A software defect in VITROS XT 7600 diagnostic systems running version 3.8.1 causes quality control baseline statistics to fail to update properly, potentially resulting in erroneous patient laboratory results.

    Product
    VITROS XT 7600 Integrated System, Catalog No. 6844461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1237-2024·2024-03-13

    Synthes RIA Tube Assembly Recalled for Unconfirmed Sterility

    Synthes is recalling 144 units of RIA Tube Assembly surgical instruments due to sterility failure. The devices cannot be confirmed as sterile and pose a risk of infection if used in orthopedic procedures.

    Product
    RIA Tube Assembly, minimum 520 mm length, sterile- intended for use in adults and adolescents (12-21 years) to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis, to harves
    Category
    Medical Device
    Distribution
    Distributed nationwide