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

Clear filters

26–50 of 39702

  • SevereFDA (Food)·H-0092-2027·2026-10-21

    Deano's Pasta Recalls Pear and Pecorino Ravioli for Undeclared Lobster

    Deano's Pasta is recalling Pear and Pecorino Triangoli Ravioli because the product contains undeclared lobster, a major food allergen.

    Product
    Deano's Pasta; Pear and Pecorino Triangoli Ravioli, 1lb.; Ingredients: Dough: Semolina (Wheat, Niacin, Thiamine, Mononitrate, Riboflavin, Folic Acid), Water, Fresh Eggs, Salt. Filling: Pears, Ricotta (Whey, Cream, Milk), Pecorino Cheese (Milk, Cultures, Salt, Enzymes)…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0002-2027·2026-10-21

    Instrumentation Laboratory Recalls HemoslL AcuStar HIT-lgG In Vitro Diagnostic Reagents

    Instrumentation Laboratory is recalling 1,414 units of HemoslL AcuStar HIT-lgG(PF-4) in vitro diagnostic reagents due to a potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.

    Product
    HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0135-2027·2026-10-21

    JenaValve Trilogy Delivery Catheter Recalled for Sleeve Liner Separation

    Jenavalve Technology Inc. is recalling 108 units of the JenaValve Trilogy Delivery Catheter due to a defect that may prevent heart valve deployment.

    Product
    JenaValve Trilogy Delivery Catheter, Size 25MM REF: TRILOGY-DC-M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0138-2027·2026-10-21

    Medtronic Recalls Grafton DBM Products Due to Donor Microbial Presence

    Medtronic is recalling specific Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.

    Product
    Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0161-2027·2026-10-21

    Beckman Coulter IQ200 Hematology Analyzers Recalled for Check Valve Defect

    Beckman Coulter is recalling IQ200 SPRINT, SELECT, and ELITE hematology analyzers because a check valve defect may cause fluid leaks, creating slip, chemical, and biohazard risks.

    Product
    IQ200 SPRINT, REF: 700-3322,700-3322RFB, 700-3325, 700-3326, B48997; IQ200 SELECT, REF: 700-3340, 700-3345, 700-3347, B48998, C10684; IQ200 ELITE, REF: 700-3370, 700-3375, 700-3375RFB, 700-3376, B48999, C10683
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V687000·2026-10-20

    Lexus NX Vehicles Recalled for Instrument Panel Display Failure

    Toyota is recalling 2022-2024 Lexus NX vehicles because the instrument panel may fail to display critical warnings, increasing crash risk.

    Product
    LEXUS — 2023 LEXUS NX PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V688000·2026-10-20

    Ford Recalls Lincoln Hybrid Vehicles for Transmission Defect

    Ford is recalling 2026-2027 Lincoln Nautilus and 2027 Corsair Hybrids because corrosion may cause the vehicle to unexpectedly shift into neutral while driving.

    Product
    LINCOLN — LINCOLN CORSAIR HYBRID, NAUTILUS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E073000·2026-10-20

    Ford Recalls ABS Modules With Incorrect Software Programming

    Ford is recalling certain Anti-Lock Brake System (ABS) modules that may have incorrect software, potentially degrading brake balance and increasing stopping distance.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V693000·2026-10-20

    Hyundai Recalls 2026 Models for Wheel Lug Nut Loosening Risk

    Hyundai is recalling 2026 Venue, Elantra N, Elantra Hybrid, and Elantra vehicles because wheel lug nuts may loosen, allowing the wheel to detach.

    Product
    HYUNDAI — HYUNDAI ELANTRA, ELANTRA HYBRID, VENUE, ELANTRA N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V685000·2026-10-19

    Subaru Recalls 2026 Forester and Crosstrek for Ball Joint Defect

    Subaru is recalling 2026 Forester and Crosstrek vehicles because a loose ball joint may separate, causing loss of control. Owners should not drive until repaired.

    Product
    SUBARU — SUBARU CROSSTREK, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2026·2026-10-17

    Kayem Foods Recalls Ready-to-Eat Meat and Poultry Due to Temperature Abuse

    Kayem Foods Inc. is recalling approximately 1.6 million pounds of ready-to-eat meat and poultry products because they may have experienced temperature abuse during storage.

    Product
    Kayem Foods Inc. — Kayem Foods Inc. Recalls Meat and Poultry Products Due to Possible Temperature Abuse
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V680000·2026-10-16

    Alliance RV Recalls Valor and Delta Trailers Due to Fire Risk

    Alliance RV is recalling 2025-2027 Valor and 2026-2027 Delta recreational trailers because a power cord fuse may not provide adequate circuit protection, increasing fire risk.

    Product
    ALLIANCE RV — ALLIANCE RV VALOR, DELTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V681000·2026-10-16

    Forest River Recalls 2026-2027 Cedar Creek Trailers for Fire Risk

    Forest River is recalling 2026-2027 Cedar Creek recreational trailers because a slide switch may lack proper overcurrent protection, creating a fire risk.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27024·2026-10-15

    3M Recalls Scotch Thermal Laminators Due to Fire Hazard

    3M is recalling Scotch thermal laminators because they can overheat and catch fire. Consumers should stop using the devices and contact 3M for a refund.

    Product
    Scotch™ Thermal Laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27025·2026-10-15

    HatsanUSA Recalls Blitz Air Rifles Due to Projectile Hazard

    HatsanUSA is recalling Blitz and Blitz 777 air rifles because they can fire unexpectedly, posing a risk of serious injury or death.

    Product
    Blitz and Blitz 777 air rifles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V679000·2026-10-15

    Spartan RV Chassis K2 Recalled for Fuel Hose Separation Risk

    Shyft Group is recalling 2024-2027 Spartan RV Chassis K2 vehicles because remote fuel filter hoses may separate, causing fuel leaks and engine stalls.

    Product
    SPARTAN — SPARTAN RV CHASSIS K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V677000·2026-10-15

    Volvo Recalls 2025-2026 VNL Trucks for Loose Structural Bolts

    Volvo Trucks North America is recalling 2025-2026 VNL (4) trucks because loose or missing structural bolts in the cab may reduce occupant protection during a crash.

    Product
    VOLVO — 2025 VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0013-2027·2026-10-14

    Berlin Seeds Recalls Alfalfa Sprouting Seeds for Potential E. coli and Salmonella

    Berlin Seeds is recalling alfalfa sprouting seeds due to potential E. coli and/or Salmonella contamination. The product was sold in Ohio and nationwide online.

    Product
    Berlin Seeds Alfalfa Sprouting Seeds, packaged in 1/4 lb., 1/2 lb., 1 lb., and 5 lb. resealable bags and 50 lb. woven poly bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0027-2027·2026-10-14

    Carolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 26/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    TIRZEPATIDE/CYANOCOBALAMIN 26/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide