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

25776–25800 of 114516

  • HighFDA (Food)·F-0346-2023·2023-02-08

    Organic jackfruit recalled for undeclared sulfites in Florida

    Organic jackfruit produced by Food Castle, Inc. is being recalled due to undeclared sulfites not listed on the product label. Sulfite-sensitive consumers face potential allergic reaction risk.

    Product
    ORGANIC JACKFRUIT Nutty and Fruity Brand UNSWEETENED AND UNSULFURED NET WT. 3.5 oz. (100g) USDA ORGANIC UPC: 819496021426 8 units per case Distributed by: Food Castle Inc. Vernon, CA 90058 PRODUCT OF SRI LANKA
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1045-2023·2023-02-08

    MEDLINE UNITE Foot and Ankle Screw Recall: Intra-Operative Failure

    MEDLINE INDUSTRIES is recalling 420 units of UNITE Foot and Ankle surgical screws (Lot 810304) due to observed intra-operative failure when pre-drilled and implanted with excessive torque.

    Product
    MEDLINE UNITE FOOT & ANKLE Screw, Non-Locking, Mini T8 (2.0x8mm), REF MMSN2008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1023-2023·2023-02-08

    Medtronic Affinity Fusion Oxygenator: Temperature Monitoring Adapter May Detach

    Medtronic is recalling 2,937 Affinity Fusion Oxygenators used in cardiac surgery because the Temperature Monitoring Adapter may detach during setup or disassembly.

    Product
    Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF BB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0335-2023·2023-02-08

    Ube Ensaymada recalled for undeclared wheat allergen

    Joy Joys Bakery LLC is recalling Ube Ensaymada sold in Washington and Oregon due to undeclared wheat. The product label lists flour but does not specify wheat flour.

    Product
    Ube Ensaymada, UPC 6658266481. Product is packaged in plastic clear clamshell container and there are 4 pieces per container. Ingredients: Cream Cheese, Cheese, Butter, Milk, Sugar, Salt, Water, Yeast, Flour, Egg. Joy Joy s Bakery contact information: (253) 507-5259, 11107…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0259-2023·2023-02-08

    Hand Sanitizer Recalled Due to Manufacturing Practice Deviations

    Frenda Corporation has recalled Global Care Antibacterial Hand Sanitizer due to manufacturing practice deviations. The recall affects 124 bottles with lot number C013121 distributed in Puerto Rico.

    Product
    Global Care Antibacterial Hand Sanitizer Alcohol Etilico 70% Original, 1 Gallon (128 FL OZ) 3785.41 mL, Dist. by Target Price, Inc. Catano, PR, UPC 8 70373 01326 2
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1044-2023·2023-02-08

    Biopsy Medium for In Vitro Fertilization Recalled Due to Product Contamination

    CooperSurgical is recalling a lot of Biopsy Medium used in IVF procedures because the product may contain an incorrect medium that could degrade embryos. No illnesses have been reported.

    Product
    BIOPSY MEDIUM 10ML, Reference Number 10620010 A, used for blastomere biopsy of cleavage stage embryos for Pre-implantation Genetic Diagnosis (PGD)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1039-2023·2023-02-08

    Non-Invasive Patient Tracker Verification Failure During Image-Guided Surgery

    Medtronic is recalling AxiEM Non-Invasive Patient Trackers due to increasing complaints that users cannot verify their navigation instruments work properly during image-guided surgery. The verification failure affects approximately 1,867 devices worldwide.

    Product
    AxiEM" Non-Invasive Patient Tracker
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-1037-2023·2023-02-08

    Turbett Surgical Container TS1200 Recalled Due to Potential Weld Failures

    Turbett Surgical Container TS1200 units may have weld failures that could breach the sterile barrier, potentially allowing unsterile instruments to be used in medical procedures and risking infection.

    Product
    Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2023·2023-02-08

    Medtronic Perfusion Oxygenator Temperature Monitoring Adapter Detachment Recall

    Medtronic has recalled Custom Pack Perfusion Tubing Packs used in cardiopulmonary bypass procedures. The Temperature Monitoring Adapter on the oxygenator may detach during setup or disassembly.

    Product
    Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF CB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1042-2023·2023-02-08

    Vanguard Knee System Prosthesis Components Incorrectly Labeled for Size and Side

    Biomet is recalling 157 units of Vanguard Knee System prosthesis components incorrectly labeled as different sizes or surgical sides. Surgeons relying on labels could implant the wrong size or side, requiring corrective surgery.

    Product
    (1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item…
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-0327-2023·2023-02-08

    Frozen breakfast sandwiches and burritos recalled for undeclared milk allergen

    The Miso Brothers Inc. is recalling frozen breakfast sandwiches and breakfast burritos containing undeclared milk, affecting approximately 31,092 units distributed throughout US retail locations. This poses a risk to consumers with milk allergies.

    Product
    Alpha Plant-Based Breakfast Sandwich - Meatless Sausage, Plant-Based Egg & Cheeze 5 oz. UPC 810070350093 Frozen
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1032-2023·2023-02-08

    Non-sterile procedural trays with potential sterile packaging breach

    Medline Industries is recalling non-sterile procedural trays containing sterile blades that may damage sterile packaging due to blade puncture risk. Lot 22IBQ980. No illnesses reported.

    Product
    Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0326-2023·2023-02-08

    Plant-based breakfast burritos recalled for undeclared milk allergen

    THE MISO BROTHERS INC is recalling 31,092 units of frozen Alpha Plant Based Breakfast Burritos due to undeclared milk. The product may contain milk, a common allergen.

    Product
    Alpha Plant Based Breakfast Burrito - Meatless Sausage SCRAMBLE 5.5 oz UPC 855099007733 Frozen
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1048-2023·2023-02-08

    GORE CARDIOFORM Septal Occluder Recalled for Incomplete Quality Documentation

    W L Gore & Associates is recalling 14 units of the GORE CARDIOFORM Septal Occluder (GSX0030A) due to incomplete quality test documentation. The missing verification of device release could pose a potential risk of device failure and serious complications.

    Product
    GORE CARDIOFORM Septal Occluder, REF: GSX0030A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-02082023-01·2023-02-08

    Goulart's Smoked Linguica Links Recalled for Undeclared Milk Allergen

    USDA FSIS issued a public health alert for Goulart's Smoked Linguica Links due to undeclared milk. Consumers with dairy allergies should not consume these products.

    Product
    Goulart's Sausage Co. — FSIS Issues Public Health Alert for Ready-To-Eat Pork Sausage Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0262-2023·2023-02-08

    Diltiazem Hydrochloride extended-release capsules recalled due to failed quality specifications

    Sun Pharmaceutical is recalling Diltiazem Hydrochloride Extended-Release Capsules (360 mg) due to failed impurity specifications and dissolution testing found during FDA laboratory evaluation. The recall affects five lot numbers distributed nationwide.

    Product
    DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2023·2023-02-08

    SynCardia Total Artificial Heart System Recalled for Cannula Tears

    SynCardia Systems is recalling its Total Artificial Heart System due to reported tears in the cannula caused by wear and tear stress. Approximately 1,732 systems worldwide are affected.

    Product
    SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2023·2023-02-08

    Turbett Surgical Container TS1000 may have weld failures breaching sterile barrier

    Turbett Surgical Container TS1000 may have weld failures that breach the sterile barrier, potentially resulting in unsterile instruments being used in medical procedures and risking patient infection or injury.

    Product
    Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1047-2023·2023-02-08

    Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk

    Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.

    Product
    MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2023·2023-02-08

    Non-sterile procedural trays risk sterile packaging breach

    Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.

    Product
    Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1029-2023·2023-02-08

    MEDLINE procedural trays recalled for potential sterile packaging breach

    MEDLINE is recalling procedural trays because sterile blades within the kits could puncture the outer foil packaging, potentially breaching the sterile barrier.

    Product
    Non-sterile procedural trays labeled as CRANI, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23115·2023-02-08

    Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk

    Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.

    Product
    Fabuloso Multi-Purpose Cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0339-2023·2023-02-08

    Daim Swedish Almond Cake Recalled for Metal Contamination

    Almondy AB is recalling Daim Swedish almond cake (NET WT 14.1oz) due to discovery of a metal object in the product. Consumers should not eat affected cakes.

    Product
    Daim, Swedish almond cake with chocolate and crunchy caramel, Baked by Almondy, NET WT 14.1oz (400g)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1027-2023·2023-02-08

    Temperature Monitoring Adapter Detachment in Cardiopulmonary Bypass Oxygenators

    Medtronic is recalling cardiopulmonary bypass equipment because the Temperature Monitoring Adapter can come loose during setup or disassembly, potentially compromising temperature monitoring during heart surgery.

    Product
    Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF BB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1043-2023·2023-02-08

    Biomet Vanguard Knee Implant Components Recalled for Incorrect Labeling

    Biomet, Inc. is recalling specific Vanguard Knee System prosthetic components that are incorrectly labeled with wrong sizes and sides. This labeling error could result in incorrect implant placement during knee replacement surgery.

    Product
    (1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement prostheses. Item Number: 183122 EXPANDED RECALL: (2) Vanguard Knee System PS Open Box Femoral; Left; 60 mm. Item Number: 183124 (3) Vanguard Knee System PS Open Box Femoral…
    Category
    Medical Device
    Distribution
    6 states