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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

21401–21425 of 114370

  • HighFDA (Food)·F-1374-2023·2023-08-16

    Bellingham Pasta Co Semolina Shells Recalled for Undeclared Wheat Allergen

    Bellingham Pasta Co is recalling Semolina Shells due to undeclared wheat. The product label does not declare wheat, posing a risk to consumers with wheat allergies.

    Product
    Semolina Shells, net wt. 13oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00219 4.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1375-2023·2023-08-16

    Bellingham Pasta Semolina Spinach Fettuccine Recalled for Undeclared Wheat Allergen

    Bellingham Pasta Co. is recalling 38 packages of Semolina Spinach Fettuccine sold in Washington because the label does not declare wheat, a major allergen present in the product.

    Product
    Semolina Spinach Fettuccine, net wt. 14oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, Organic Spinach Powder, dusted with Brown Rice Flour. Keep Refrigerated. UPC…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2348-2023·2023-08-16

    Medical Device Recall: LINK MP Hip Stem Trial Instruments Removal Difficulty Risk

    Waldemar Link GmbH recalls LINK MP Monoblock hip stem trial instruments due to increased removal force requirements after impaction, which may prolong surgery or require procedural modification.

    Product
    LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 17 - indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-117/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1378-2023·2023-08-16

    Semolina linguine pasta recalled for undeclared wheat allergen

    Bellingham Pasta Co is recalling semolina linguine due to missing wheat allergen declaration on the label. Consumers with wheat allergies may be at risk.

    Product
    Semolina Linguine, net wt. 14oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00204 0.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2346-2023·2023-08-16

    LINK MP Monoblock Hip Stem trial instruments recalled for difficulty in removal

    Waldemar Link is recalling 24 LINK MP Monoblock Hip Stem trial instruments due to increased force required to remove them after impaction, which may prolong surgery or require procedure modification.

    Product
    LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 15 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 136-115/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2358-2023·2023-08-16

    FDA Recalls Troponin Cardiac Test Calibrators for Potential False Negatives

    Ortho-Clinical Diagnostics is recalling VITROS Troponin I ES Calibrators because reagent packs may contain incorrect wells that could produce false negative results. The recall affects 4,013 units distributed worldwide.

    Product
    VITROS Immunodiagnostic Products Troponin I ES Calibrators
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1390-2023·2023-08-16

    Sweet Alchemy ice cream recalled for undeclared allergens

    Sweet Alchemy Strawberry Rhubarb Crisp ice cream sold in Washington has been recalled because its labels do not declare the presence of milk, egg, and wheat allergens.

    Product
    Sweet Alchemy Strawberry Rhubarb Crisp ice cream, distributed in cups and pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1367-2023·2023-08-16

    Bellingham Pasta Co Linguine Recalled Due to Undeclared Wheat Allergen

    Bellingham Pasta Co is recalling 190 packages of Semolina Lemon Black Pepper Linguine because the label declares semolina flour but fails to declare wheat as an ingredient, posing a risk to consumers with wheat allergies.

    Product
    Semolina Lemon Black Pepper Linguine, net wt. 14oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, Lemon, Black Pepper, dusted with Brown Rice Flour. Keep…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1368-2023·2023-08-16

    Semolina Vegan Rigatoni Pasta Recalled for Undeclared Wheat Allergen

    Bellingham Pasta Co is recalling Semolina Vegan Rigatoni due to undeclared wheat allergen in the semolina flour ingredient.

    Product
    Semolina Vegan Rigatoni, net wt. 13oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00234 7.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1373-2023·2023-08-16

    Semolina Gemelli Pasta Recall for Undeclared Wheat Allergen

    Bellingham Pasta Co. is recalling Semolina Gemelli pasta because the label does not declare wheat, a major allergen, despite wheat being an ingredient. Consumers with wheat allergies should not consume this product.

    Product
    Semolina Gemelli, net wt. 13oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00227 9.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2349-2023·2023-08-16

    Hip Stem Trial Instrument Difficult to Remove After Impaction

    LINK MP Monoblock hip stem trial instruments may require increased force to remove after impaction, potentially prolonging surgery or requiring procedure modification. No injuries or illnesses have been reported.

    Product
    LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 18 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-118/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2363-2023·2023-08-16

    Surgical Spinal Tap Device Recalled for Incorrect Laser Marking

    Medtronic is recalling Solera Awl Tip Tap surgical devices due to incorrect laser marking. Thirteen devices were distributed in Florida, Colorado, Indiana, South Carolina, Texas, and Utah.

    Product
    CD HORIZON Spinal System Solera Awl Tip Tap, REF NAV2006K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2365-2023·2023-08-16

    Medtronic InterStim Ground Pad Recalled for Incorrect Expiration Date Label

    Medtronic is recalling InterStim Self-Adhesive Ground Pad (lot 60347246) due to incorrect expiration date labeling. Affected units were distributed internationally including to Iran.

    Product
    Medtronic InterStim Ground Pad REF 041826
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2343-2023·2023-08-16

    Olympus Endoscope Reprocessor OER-Mini Labeling Revised for Device Compatibility

    Olympus revised labeling for the OER-Mini endoscope reprocessor. The company removed LF-V and LF-P endoscopes from the list of compatible devices and updated sterilization procedures.

    Product
    Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1082-2023·2023-08-16

    Dofetilide Capsules Recalled Due to Out-of-Specification Content Uniformity

    Sun Pharmaceutical recalls Dofetilide 500 mcg capsules nationwide due to out-of-specification results in content uniformity testing. Affected lot DNE0217A with expiration 01/2025 may not meet pharmaceutical specifications.

    Product
    DOFETILIDE — DOFETILIDE (DOFETILIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2392-2023·2023-08-16

    Canon Medical INFX-8000C Tableside Console PWB Requires Replacement

    Canon Medical has recalled 12 INFX-8000C tableside consoles due to a printed circuit board that may require replacement. Though procedures may be delayed, x-ray operations can continue using alternative controls.

    Product
    INFX-8000C XGCP-930AA TABLE SIDE CONSOLE, INFX-8000C XGCP-930BA TABLE SIDE CONSOLE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2400-2023·2023-08-16

    MR 7700 Magnetic Resonance System Diagnostic Cable Installation Defect

    Philips MR 7700 Magnetic Resonance systems may have an improperly installed diagnostic cable. The cable does not impact system functionality or patient safety.

    Product
    MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2353-2023·2023-08-16

    LINK MP Hip Stem Difficult to Remove After Surgical Implantation

    Waldemar Link is recalling LINK MP Monoblock hip stem prosthetics that may require increased force to remove after surgical implantation, potentially prolonging surgery.

    Product
    LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 22 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-22/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2399-2023·2023-08-16

    MRI System Cable Installation Issue During Service Setup

    Philips Ingenia Elition S MR systems may have an improperly installed cable connecting the SmokeDetector Interlock to the host PC. This affects service diagnostics only and does not impact system functionality.

    Product
    Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2398-2023·2023-08-16

    Philips Ingenia Elition X MR Systems Diagnostic Cable Installation Issue

    Philips is recalling 601 Ingenia Elition X MR systems because a diagnostic cable may not have been properly installed, though system operation is not affected.

    Product
    Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·037-2023·2023-08-15

    Bellboy Import Recalls Frozen Raw Pork Belly for Import Violation

    Bellboy Import Corporation is recalling approximately 551 pounds of frozen, raw pork belly because the products were not presented for import reinspection into the United States.

    Product
    Bellboy Import Corporation Recalls Frozen, Raw Pork Products Produced Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·23V582000·2023-08-15

    2023 Indian Pursuit Limited Fuel Line Assembly Defect Recall

    Indian Motorcycle Company is recalling 2023 Pursuit Limited motorcycles because the fuel line may have been improperly assembled. This can cause engine stall and increase the risk of a crash.

    Product
    INDIAN — INDIAN PURSUIT LIMITED, CHALLENGER, PURSUIT DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V581000·2023-08-15

    2020-2022 Nissan Sentra Recalled for Bent Steering Tie Rod

    Nissan North America is recalling 2020-2022 Sentra vehicles because the left or right tie rod may bend, potentially breaking and causing loss of steering control. Owners should contact their dealer for free interim repairs.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V579000·2023-08-15

    2023 Kia Sorento Recalled for Detachable Air Bag Warning Labels

    Kia is recalling certain 2023 Sorento vehicles. Air bag warning labels on sun visors may detach, preventing occupants from being warned about air bag deployment risks in a crash.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide