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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Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

826–850 of 89448

  • SevereFDA (Drugs)·D-0673-2026·2026-07-15

    Bortezomib for Injection Recalled Due to Lack of Sterility Assurance

    Bortezomib for Injection 3.5mg/Vial manufactured by Reliance Life Sciences is being recalled nationwide due to lack of sterility assurance. Affected lots include RBIH0125A, RBIH0225A, RBIH0325A, and RBIH0525A distributed across the USA.

    Product
    Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1148-2026·2026-07-15

    Fresh to You Burger Chicken Fillet Deluxe with Bacon Recalled

    Fresh to You Burger Chicken Fillet Deluxe with Bacon (SKU 10303) is being recalled because raw breaded chicken patties were inadvertently used instead of cooked patties, posing a risk of Salmonella contamination.

    Product
    Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2716-2026·2026-07-15

    TMINI Tracking Array knob loosening causing potential array misalignment

    Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays used in knee replacement surgery because the knob on the tracking array may loosen, causing potential misalignment of the array.

    Product
    TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0671-2026·2026-07-15

    Pemetrexed for Injection Recalled Due to Lack of Sterility Assurance

    Somerset Therapeutics is recalling Pemetrexed for Injection 100mg/Vial due to lack of sterility assurance. The recall affects approximately 12,000 vials distributed nationwide.

    Product
    Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V454000·2026-07-15

    E-One Recalls Emergency Vehicles Due to Drive Mode Transfer Case Defect

    E-One is recalling 2025-2026 Cyclone N, Typhoon N, and Commercial emergency vehicles because the drive/pump mode transfer case may disengage, causing loss of rear-wheel power.

    Product
    E-ONE — E-ONE COMMERCIAL, CYCLONE N, TYPHOON N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1140-2026·2026-07-15

    EC Hot Links Seasoning 45.05# Recalled for Undeclared Sesame

    Adams Extract & Spice LLC is recalling EC Hot Links Seasoning 45.05# due to undeclared sesame allergen. The product may pose a serious health risk to consumers with sesame allergies.

    Product
    EC Hot Links Seasoning 45.05#
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2712-2026·2026-07-15

    Elekta Geneva Brachytherapy Applicator Intrauterine Tube Detachment Risk

    Elekta is recalling the Geneva Brachytherapy Applicator due to a safety concern that the tip of the intrauterine tube may detach and remain inside a patient during cancer treatment.

    Product
    Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0672-2026·2026-07-15

    Pemetrexed for Injection recalled due to lack of sterility assurance

    Reliance Life Sciences is recalling Pemetrexed for Injection 500mg/Vial nationwide due to lack of sterility assurance. The affected product may not meet required sterility standards for intravenous use.

    Product
    Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2711-2026·2026-07-15

    Brachytherapy Applicator Advanced Gynecological Applicator Tip Detachment

    Elekta, Inc. is recalling Advanced Gynecological Applicators due to potential detachment of the intrauterine tube tip, which may remain inside a patient during cancer treatment.

    Product
    Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1150-2026·2026-07-15

    High Valley Orchard Chocolate Covered Raisins Recalled for Undeclared Peanut

    High Valley Orchard Chocolate Covered Raisins (15oz bags) are recalled nationwide due to undeclared peanut from mis-packaging. Consumers with peanut allergies should not consume this product.

    Product
    High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is packaged in clear plastic container. UPC on retail container: 0 952348 80170 0. The label of affected product declares: INGREDIENTS: MILK CHOCOLATE (SUGAR,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2715-2026·2026-07-15

    VITEK 2 AST-N447 Test Kit Potentially Returns False Resistant Results

    Biomerieux Inc is recalling VITEK 2 AST-N447 TEST KIT (Lot 0853293604) distributed internationally due to potential false resistant carbapenem and/or cephalosporin results when pouch foil fractures are present.

    Product
    VITEK 2 AST-N447 TEST KIT Product reference 424620
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-1147-2026·2026-07-15

    Alabama Banana Pudding Marshmallow Recall Due to Metal Contamination

    Wondermade LLC is recalling Alabama Banana Pudding Marshmallow products because they may contain small metal pieces. The affected 4-ounce boxes were distributed to Pennsylvania, Texas, Indiana, and Florida.

    Product
    Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged in a sealed plastic bag inside a printed cardboard box
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·H-1142-2026·2026-07-15

    Johnny's Salad and Pasta Elegance products recalled for undeclared sesame allergen

    Adams Extract & Spice LLC is recalling Johnny's Salad and Pasta Elegance seasoning products because they contain undeclared sesame, a known allergen. The recall affects two product sizes distributed in Texas.

    Product
    Johnny's Salad and Pasta Elegance 5.5 oz (UPC: 0-70381-10014-9) " Johnny's Salad and Pasta Elegance 2.75 oz (UPC: 0-70381-10013-2)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-1138-2026·2026-07-15

    Smoked Sausage Spice recalled for undeclared sesame allergen

    Adams Extract & Spice LLC is recalling Smoked Sausage Spice due to undeclared sesame allergen. Consumers with sesame allergies should not use the affected product.

    Product
    Smoked Sausage Spice 32.86#
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-1143-2026·2026-07-15

    Bakr Brown Butter Chocolate Chunk Cookie Dough Recalled for Undeclared Soy

    Bear Stewart Co is recalling Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough due to undeclared soy. The product was distributed in Southern California, Southern Nevada, Arizona, and Utah through Target stores.

    Product
    Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough, 8-oz pouch 12 cookies per pouch, UPC 8 50073 08700 8, 8 pouches per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2698-2026·2026-07-15

    MiniMed 780G Insulin Pump Software Anomaly Recall

    Medtronic MiniMed's 780G Insulin Pump can stop delivering insulin due to a software anomaly when paired with the Instinct sensor, potentially leading to delayed therapy and increased risk of hyperglycemia or diabetic ketoacidosis.

    Product
    MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2703-2026·2026-07-15

    Atellica CH Enzymatic Hemoglobin A1c assay well-to-well bias

    Siemens is recalling an A1c blood test assay (Material Number 11097536) for the Atellica CH and Atellica CI analyzers due to potential intermittent bias that could cause falsely high or low hemoglobin A1c patient results.

    Product
    Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2694-2026·2026-07-15

    Intracept Access Instruments sterile barrier breach risk

    Boston Scientific is recalling Intracept Access Instruments due to potential sterile barrier breach in the outer tray seal, which could introduce infection risk.

    Product
    Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1145-2026·2026-07-15

    Vanilla Dessert Shells Recalled for Undeclared Soy Allergen

    Specialty Bakers, LLC is recalling Vanilla Dessert Shells (Giant) because they contain soy that is not declared on the label, posing a risk to consumers with soy allergies.

    Product
    Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 grams. 1package is 142 grams. 1 package has 1 plastic tray which holds 6 desserts shells. Plastic is wrapped around 1 tray. 24 packs/Case. Frozen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-1139-2026·2026-07-15

    JB Chicken Sknls 35.73# Recalled for Undeclared Sesame Allergen

    Adams Extract & Spice LLC is recalling JB Chicken Sknls 35.73# due to undeclared sesame allergen. Consumers with sesame allergies who consume the product face a risk of allergic reaction.

    Product
    JB Chicken Sknls 35.73#
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·26E046000·2026-07-14

    Ford Recalls Integrated Trailer Brake Control Kits for F-150s

    Ford is recalling specific integrated trailer module accessory kits for 2021-2026 F-150s because they may lose communication, causing a loss of trailer brakes and lights.

    Product
    EXTERIOR LIGHTING:TAIL LIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide