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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51–75 of 90166

  • 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
  • SevereNHTSA·26V695000·2026-10-21

    BMW Recalls 2018-2020 Models for Loose Battery Cable Fire Risk

    BMW is recalling certain 2018-2020 530e and 740Le vehicles because a loose positive battery cable on the engine starter can spark and cause a fire.

    Product
    BMW — BMW 530E XDRIVE IPERFORMANCE, 740LE XDRIVE IPERFORMANCE, 530E IPERFORMANCE
    Category
    Vehicle
    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
  • HighFDA (Devices)·Z-0170-2027·2026-10-21

    Medline Recalls Surgical Convenience Kits with Non-Conforming Cannula Components

    Medline is recalling 193,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) OPEN HEART CDS, Medline product number/SKU CDS840094R; 2) OPEN HEART CDS, Medline product number/SKU CDS840171AG; 3) MHC AV FISTULA, Medline product number/SKU DYNJ903705K; 4) PERIPHERAL VASC MAJR-LF, Medline product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0177-2027·2026-10-21

    Medline Recalls Surgical Kits With Non-Conforming Cannula Components

    Medline Industries is recalling 1,900 surgical convenience kits because cannula components do not meet ISO 80369-7 standards and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product Number/SKU DYNJ80055A; 2) AV SHUNT PACK-LF, Medline Product Number/SKU DYNJ24528M.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0090-2027·2026-10-21

    Saratoga Potato Chips Recalls J. HIGGS Loaded Bacon & Cheddar Chips

    Saratoga Potato Chips LLC is recalling J. HIGGS Loaded Bacon & Cheddar Potato Chips due to undeclared soy. The product was sold in Save A Lot stores in six states.

    Product
    J. HIGGS Loaded Bacon & Cheddar Potato Chips, NET WT 7.75 OZ (219.7g) bag, UPC 051933316454. Sold as 13 (7.75oz) bags per case.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0151-2027·2026-10-21

    Baxter Recalls Likorall Overhead Lifts Due to Motor Shaft Breakage Risk

    Baxter Healthcare is recalling Likorall Overhead Lifts because a motor shaft breakage combined with reduced safety system performance may cause the lift strap to lower quickly, posing a risk of patient injury.

    Product
    Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122005NA Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122006 Product Description…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0139-2027·2026-10-21

    BD Phoenix Panel NMIC-312 recalled for classification error

    Becton Dickinson is recalling 553,625 BD Phoenix Panel NMIC-312 units nationwide because the CPO Ambler classification feature may misclassify Klebsiella pneumoniae.

    Product
    BD Phoenix Panel NMIC-312. Catalog Number: 449082.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V699000·2026-10-21

    Autocar Recalls Xpeditor Trucks for Fuel Hose Separation Risk

    Autocar is recalling 2022-2027 Xpeditor trucks with Cummins L9 engines because fuel hoses may separate, causing leaks, engine stalls, and fire risks.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0171-2027·2026-10-21

    Medline Recalls Surgical Kits With Non-Conforming Cannula Components

    Medline Industries is recalling 8,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF, Medline product number/SKU DYNJ0826732J; 2) NBMC VASCULAR PACK-LF, Medline product number/SKU DYNJ0665837G; 3) AV FISTULA, Medline product number/SKU DYNJ900454C; 4) VEIN PACK SHD, Medline product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0179-2027·2026-10-21

    Medline surgical kits recalled for non-conforming cannula components

    Medline is recalling 6,069 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) SPINAL CDS, Medline Product Number/SKU CDS940087AM; 2) CUSTOM CRANI, Medline Product Number/SKU DYNJ907697C; 3) FEM POP PACK-LF, Medline Product Number/SKU DYNJ0159820F; 4) AV FISTULA PACK, Medline Product Number/SKU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V697000·2026-10-21

    Thomas Built Buses Recalls 2027 Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses because a heater hose may rupture, causing hot coolant to leak and burn occupants.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    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 — LEXUS NX PLUG-IN HYBRID, NX HYBRID, NX
    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 NAUTILUS HYBRID, CORSAIR 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
  • HighNHTSA·26V689000·2026-10-20

    Ford Recalls F-Series Trucks Due to Tailgate Cable Failure Risk

    Ford is recalling certain 2026-2027 F-Series trucks because a tailgate cable may fail under heavy loads, posing an injury risk.

    Product
    FORD — FORD F-150, F-450 SD, F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E074000·2026-10-20

    Great Dane Trailer Landing Gear Recall Due to Weld Failure Risk

    Great Dane Trailers is recalling specific landing gear assemblies because k-brace welds may fail, causing the gear to collapse and increasing injury risk.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER:HOSES/CABLES/RODS/GEARS/STRUT/CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V686000·2026-10-20

    Forest River Recalls 2023-2026 Pause Travel Trailers for Wiring Defect

    Forest River is recalling 2023-2026 Pause travel trailers because an incorrect connector was used for 12-volt solar panel wires, which may increase the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER PAUSE
    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 — 2026 SUBARU 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