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

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

9676–9700 of 31231

  • HighFDA (Devices)·Z-0688-2025·2024-12-25

    K-Systems G85 Mini Incubator May Exceed Desired Temperature

    CooperSurgical recalls 37 K-Systems G85 Mini Incubators because the device warming surfaces may exceed the desired set temperature. The unit alarms when this occurs, but affected serial numbers require verification.

    Product
    Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-0285-2025·2024-12-25

    Impossible Spicy Ground Sausage Recalled for Potential Metal Contamination

    Impossible Foods is recalling Impossible Spicy Ground Sausage due to potential metal pieces in the product. The recall affects 32,536 cases distributed nationwide with use-by dates between June 28, 2025 and January 28, 2026.

    Product
    Impossible Spicy Ground Sausage Meat from plants 14oz chub, UPC 8 16697 02109 5; 8 retail chubs per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0312-2025·2024-12-25

    L'Oven Fresh KETO Tortilla Wraps Recalled for Metal Contamination

    L'Oven Fresh KETO Friendly Multiseed 6 Tortilla Wraps are being recalled due to potential metal contamination. Products were distributed in CT, KS, MN, OH, and TX.

    Product
    L'Oven Fresh KETO Friendly Multiseed 6 Tortilla Wraps. Net Wt. 7.8 oz(222g) UPC 4099100271355. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510. Product of Canada
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-0152-2025·2024-12-25

    Ophthalmic solution recalled for lack of sterility assurance

    Regener-Eyes ophthalmic solution is being recalled due to lack of sterility assurance. Approximately 170,812 bottles distributed nationwide are affected.

    Product
    REGENER-EYES — REGENER-EYES (GLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2025·2024-12-25

    Cucumber Products Recalled Due to Potential Salmonella Contamination

    Indianapolis Fruit Company is recalling 288 cases of cucumber products distributed to Indiana, Kentucky, Ohio, and Pennsylvania due to potential salmonella contamination.

    Product
    Cucumbers Slices 1/2 Cup, 100 cups per case, Product Code CUCS100, Item Number - 14705 Cucumbers Diced 1" Peeled 5 lb. tray, 2 trays per case, Product Code CUDN45L, Item Number - 9975 Cucumbers Slices 2 oz., 100 per case, Product Code CUS100, Item Number - 9816 Cucumbers Slices
    Category
    Food
    Distribution
    4 states
  • HighFDA (Drugs)·D-0140-2025·2024-12-25

    Dental City Topical Anesthetic Gel Recalled Due to Manufacturing Defect

    Dental City Topical Anesthetic Gel (Benzocaine 20%) is recalled because the product was released and distributed despite failing quality inspection. Scratches were found in the mixing vessel during routine inspection.

    Product
    Dental City, Topical Anesthetic Gel, Benzocaine 20%, Net Content: 1 oz. (30 ml), Gluten Free, Manufactured for: Dental City, Green Bay, WI 54311, dentalcity.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0709-2025·2024-12-25

    Medical Imaging Software Recall: mint Lesion Orientation Display Malfunction

    Mint Medical is recalling mint Lesion software versions 3.9.0–3.9.5 due to a malfunction that may display incorrect orientation labels for certain medical images. 65 units were distributed in the US and internationally.

    Product
    mint Lesion, Software Versions: 3.9.0 through 3.9.5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0702-2025·2024-12-25

    Hillrom Temperature Management Controller Power-On Self-Test Error Code Update

    Augustine Temperature Management recalled Hillrom Temperature Management Controllers (Models WC71, WC77, and MP 2083516) due to power-on self-test error code EA POST. No injuries or illnesses reported.

    Product
    Hillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0693-2025·2024-12-25

    Bronchoscopic system may lose power due to defective component

    A defective power component in Noah Medical's Galaxy System bronchoscope may cause sudden power loss during procedures, potentially leading to lung injury or pneumotharax.

    Product
    Galaxy System (GAL-001)
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-0306-2025·2024-12-25

    Griffith Foods Italian Style Herb Powder Recalled for Metal Contamination

    Griffith Foods has recalled Item 79588401 (Italian Style Herb Powder) in 55 lb bags due to potential metal pieces. Affected lots 577773 and 577774 were distributed to IL, NY, NC, WI, TX, TN, and GA.

    Product
    Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0657-2025·2024-12-25

    Ambler Surgical Bipolar Pencil recalled for outer tube structural failure

    Kirwan Surgical Products is recalling the Ambler Surgical Bipolar Pencil 25 Gauge Straight (Model PD7226) because the outer stainless-steel tube may break or detach during use. 4,470 units worldwide are affected.

    Product
    Ambler Surgical Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: PD7226. The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization of the retinal area durin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0153-2025·2024-12-25

    OTC Ophthalmic Solution Recalled for Lack of Sterility Assurance

    REGENER-EYES ophthalmic solution is being recalled nationwide due to lack of sterility assurance. Consumers should stop using affected lots immediately.

    Product
    REGENER-EYES — REGENER-EYES (REGENER-EYES)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0304-2025·2024-12-25

    Spicy Breading Product Recalled for Potential Metal Contamination

    GRIFFITH FOODS LTD has recalled 50-pound bags of Spicy Breading Export (LOT 575830) due to potential metal contamination. Affected product was distributed to IL, NY, NC, WI, TX, TN, and GA.

    Product
    Item 42081001, 104023600 SPICY BREADING EXPORT, 50 lb. bag
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-0146-2025·2024-12-25

    Quala Dental Topical Anesthetic Gel Recalled for Manufacturing Equipment Defect

    Quala Dental Products topical anesthetic gel (20% benzocaine) is recalled due to manufacturing equipment defects. The bulk product was inadvertently released despite Quality Unit rejection after inspection found scratches on the mixing vessel.

    Product
    Quala Dental Products, Topical Anesthetic Gel, Contains 20% Benzocaine, Net Contents: 1 oz (30g), Gluten Free, Quala Dental Products, Made in USA for: NDC, Inc, 407 New Sanford Road, La Vergne, TN 37086, www.quala.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0705-2025·2024-12-25

    OEC 9900 Mobile Fluoroscopic X-Ray System Recall for Sealing Defect

    GE OEC Medical Systems is recalling 78 OEC 9900 Elite mobile fluoroscopy systems due to insufficient sealing of X-ray tubes. The defect can result in oil leaks and loss of fluoroscopic imaging capability.

    Product
    OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedures. Examples of clinical application ma
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-0297-2025·2024-12-25

    Bulk Candy Coated Popcorn Recalled for Undeclared Milk Allergen

    Yoder's Cashew Crunch Corn, unlabeled bulk candy coated popcorn, is being recalled because milk allergen is not declared. The product was distributed to retail and wholesale locations in Iowa and Georgia.

    Product
    Yoder's Cashew Crunch Corn, bulk candy coated popcorn packaged in clear plastic without label.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0310-2025·2024-12-25

    Bakestone Brothers Pita Bread Recalled Due to Metal Contamination

    Bakestone Brothers Pita Bread is being recalled due to the presence of metal pieces in the product. Consumers who have purchased this bread should not consume it and should discard it.

    Product
    Bakestone Brothers Pita Bread, 6 Whole Wheat Pitas. Net Wt. 11.4 oz(325g) UPC 0 57391-01002 6. Manufactured by PBF pita Bread Factory Ltd, 8000 Winston Street, Burnaby British Columbia V5A 2H5. Product of Canada
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0305-2025·2024-12-25

    Italian Meatball Dry Mix Recalled Due to Metal Contamination

    GRIFFITH FOODS LTD is recalling 25,903 pounds of Italian Meatball Dry Mix due to potential metal pieces in the product. The product was distributed across IL, NY, NC, WI, TX, TN, and GA.

    Product
    Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. bag
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0696-2025·2024-12-25

    ET Tube Holder Recalled for Risk of Facial Skin Injury

    Medline's HUDSON RCI mBrace ET tube holder is being recalled because its adhesive and frame design may put excessive pressure on patients' cheekbones and upper lip, potentially causing skin injury.

    Product
    HUDSON RCI mBrace, ET Tube Holder with Bite Block and 2 Point Head Strap, REF DYNJMBRC2B; tracheal tube fixation device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0307-2025·2024-12-25

    Griffith Foods Breader Recalled for Potential Metal Contamination

    Griffith Foods Ltd is recalling Item 25293502 Adhesion Breader EX due to potential pieces of metal in the product. The recall affects approximately 25,903 pounds distributed across multiple states.

    Product
    Item 25293502, ADHESION BREADER EX, 50 lb. bag
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0695-2025·2024-12-25

    HUDSON RCI mBrace ET Tube Holder Risks Facial Dermal Injury

    Medline is recalling the HUDSON RCI mBrace ET tube holder because defective adhesive and frame elements may cause pressure and skin injury to the face.

    Product
    HUDSON RCI mBrace, ET Tube Holder and 2 Point Head Strap, REF DYNJMBRC2; tracheal tube fixation device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0308-2025·2024-12-25

    Bulk Food Ingredient Recalled for Potential Metal Contamination

    Griffith Foods Ltd recalls bulk food ingredient Item 16354301 due to potential metal contamination. Product was distributed to food service facilities in Illinois, New York, North Carolina, Wisconsin, Texas, Tennessee, and Georgia.

    Product
    Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.115 lb. bag
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-0142-2025·2024-12-25

    FDA Recalls Health-Tec Benzocaine Topical Anesthetic Due to Manufacturing Defect

    Keystone Industries recalls Health-Tec Topical Anesthetic (Benzocaine 20%) lot BNZ-001646 due to manufacturing defects. Scratches found in the mixing vessel caused product rejection designation, but product was inadvertently shipped.

    Product
    HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0309-2025·2024-12-25

    Bakestone Brothers Pita Bread recalled for metal contamination

    Bakestone Brothers Pita Bread (6-count) is being recalled from five states due to metal fragments found in the product. Consumers should not consume the affected bread.

    Product
    Bakestone Brothers Pita Bread, 6 White Pita. Net Wt. 11.4 oz(325g) UPC 0 57391-00001 0. Manufactured by PBF pita Bread Factory Ltd, 8000 Winston Street, Burnaby British Columbia V5A 2H5. Product of Canada
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0704-2025·2024-12-25

    Fluoroscopic X-Ray System Recalled for Insufficient X-Ray Tube Sealing

    GE OEC Elite mobile fluoroscopic X-ray systems are recalled due to insufficient sealing of X-ray tubes, which can cause oil leaks and loss of imaging capability. Approximately 100 systems have been affected.

    Product
    OEC Elite REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical
    Category
    Medical Device
    Distribution
    44 states