The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

1976–2000 of 52931

  • HighFDA (Devices)·Z-1406-2026·2026-02-25

    Choice drape packs recalled over sterilization equipment calibration issues

    Medline is recalling 72 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1376-2026·2026-02-25

    Olympus Thunderbeat 5 mm Front-Actuated Grip Medical Device Recall

    Olympus Corporation of the Americas is removing Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip devices due to reports of adverse events.

    Product
    Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1395-2026·2026-02-25

    Major laparotomy kits recalled over sterilization equipment calibration issues

    Medline is recalling 82,597 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS, Model Number: CDS860015U; 2) MAJOR LAPAROTOMY CDS, Model Number: CDS860015V; 3) MAJOR LAPAROTOMY CDS, Model Number: CDS860015W; 4) MAJOR LAPAROTOMY CDS, Model Number: CDS860015X; 5) MINOR LAPAROTOMY CDS, Model Number: CD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1384-2026·2026-02-25

    Medline Convenience Kits Recalled Due to Potential Sterility Assurance Issues

    Medline Industries, LP is recalling certain Medline Convenience Kits because equipment calibration issues may have impacted the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) ANCILLARY PACK-LF, Model Number: DYNJ0185290G; 2) OPEN HEART ANESTHESIA ICC-A, Model Number: DYNJ905567A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V109000·2026-02-24

    Thomas Built Buses Recalls 2027 Saf-T-Liner C2 School Buses for Heater Hose Defect

    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 into the passenger compartment.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V107000·2026-02-24

    Newmar Recalls 2026 Freedom Aire Motorhomes Due to Wiring Defect

    Newmar is recalling 2026 Freedom Aire motorhomes because a wiring error may cause the heating system to activate unintentionally, producing harmful gas.

    Product
    NEWMAR — NEWMAR FREEDOM AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V099000·2026-02-20

    Mercedes-Benz eSprinter Recalled for Insufficient Pedestrian Warning Sounds

    Daimler Vans USA is recalling 2025 Mercedes-Benz eSprinter vehicles because they fail to make sufficient pedestrian warning sounds when in reverse, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ESPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V104000·2026-02-20

    Ford Vehicles Recalled for Integrated Trailer Module Software Defect

    Ford is recalling multiple 2021–2026 trucks, vans, and sport utility vehicles because the integrated trailer module may lose communication with the vehicle when towing, causing loss of trailer brake and turn signal lights or brake function.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR, F-600 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V102000·2026-02-20

    Orange EV Recalls T-Series and e-TRIEVER Trucks for Door Lock Defect

    Orange EV is recalling 2018-2026 T-Series and e-TRIEVER trucks because driver's side door handles may lack a lock, potentially failing federal safety standards.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK, E-TRIEVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26272·2026-02-19

    Magnetic balls and rods sets recalled over a deadly choking hazard

    About 782 Huaker Magnetic Balls and Rods sets are being recalled because they contain small balls and are intended for children under three years of age.

    Product
    Huaker Magnetic Balls and Rods Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26275·2026-02-19

    Children's footed sleepwear recalled over the flammability standard for sleepwear

    About 211,520 MCS and Lullaby Lane one-piece footed sleepwear items sold at Meijer are being recalled because they violate the mandatory flammability standard for children's sleepwear.

    Product
    Meijer one-piece footed 12-, 18-and 24-month children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V095000·2026-02-19

    Prevost Recalls 2026 H3-45 Buses Due to Mirror Detachment Risk

    Prevost is recalling 2026 H3-45 and H3-45 VIP buses because aftermarket driver-side mirrors may detach, creating a road hazard.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E008000·2026-02-19

    Prevost Recalls Exterior Driver Side Mirrors Due to Detachment Risk

    Prevost is recalling specific exterior driver side mirrors that may detach due to excessive play, posing a visibility and road hazard risk.

    Product
    VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26277·2026-02-19

    Youth helmets recalled over failure to meet positional stability requirements

    About 3,295 SAMIT youth multi-purpose helmets are being recalled because they do not comply with the positional stability and certification requirements of the bicycle helmet standard.

    Product
    SAMIT Youth Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26276·2026-02-19

    Book nook decorations recalled over an accessible spare coin battery

    About 1,770 Prismatic 3D Prints Book Nooks with Lights are being recalled because the spare lithium coin battery can be easily accessed by children.

    Product
    Prismatic 3D Prints Book Nooks with Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26274·2026-02-19

    LED balloon lights recalled over easily accessible button cell batteries

    About 3,400 JJGoo LED Balloon Lights are being recalled because children can easily access the button cell batteries and the lights lack the warnings required by Reese's Law.

    Product
    JJGoo LED Balloon Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1348-2026·2026-02-18

    Azurion 7 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1351-2026·2026-02-18

    Azurion 5 M20 systems recalled over tables that may move unexpectedly

    Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0495-2026·2026-02-18

    Spicy breakfast burritos recalled over small hard plastic fragments

    MG Foods-Compass Group is recalling 3,099 Spicy Breakfast Burritos, 10 oz, over foreign material described as small hard plastic fragments.

    Product
    Spicy Breakfast Burrito in a flour tortilla. Net Weight 10 oz (283g) Scrambled eggs, Salsa, Potatoes, Jalapenos, Cheddar, Green Pepper & Onion. UPC 1 00001-00029 7. Keep Refrigerated. Manufactured By: MG Foods, Oak Creek, WI 53154.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-0313-2026·2026-02-18

    Estradiol 22mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 133 pellets of ESTRADIOL, 22 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1339-2026·2026-02-18

    GammaPlan 11.1 recalled over plans that may irradiate the wrong location

    Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.

    Product
    Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide