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.

25151–25175 of 50443

  • HighFDA (Devices)·Z-2239-2019·2019-08-21

    BioPro K-Wire HBS Sterile Recalled for Sterile Barrier Flaw

    BioPro, Inc. is recalling 17 units of K-Wire HBS Sterile due to a manufacturing flaw in the sterile barrier system.

    Product
    K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2258-2019·2019-08-21

    BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw

    BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x38 due to a manufacturing flaw in the sterile barrier system.

    Product
    Go-EZ Screw 6.5x38, Item Number 19655 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2276-2019·2019-08-21

    NeuroLogica WS80A Diagnostic Ultrasound System Recalled for Probe Overheating Risk

    NeuroLogica is recalling WS80A Diagnostic Ultrasound Systems because probes may overheat when users decrease the Doppler Sample Volume size in Doppler Only mode.

    Product
    WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01.06, 3.01.07, 3.01.08, 3.01.09, 4.00.08, 4.00.09, 4.00.10, 4.00.11, 4.01.00, 4.01.01, 4.01.02, 4.01.03, 4.01.04, 4.01.05, 4.01.06, 4.01.07…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E055000·2019-08-20

    Hale SmartFoam 6.5-12 Foam Pump Systems Recalled for Overheating Risk

    Hale Products Inc. is recalling SmartFoam 6.5-12 foam pump systems with 12-volt power supplies because they can overheat and fail, rendering fire-fighting foam unavailable.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V610000·2019-08-20

    Newmar Recalls 2018-2020 Motorhomes Due to Falling Bedroom Fascia Header

    Newmar is recalling 2018-2020 King Aire, Mountain Aire, and Essex motorhomes because the bedroom fascia header may fall onto the bed, increasing injury risk.

    Product
    NEWMAR — NEWMAR ESSEX, MOUNTAIN AIRE, KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19769·2019-08-19

    Club Car Recalls Gas Utility Vehicles Due to Fuel Leak Fire Risk

    Club Car is recalling approximately 1,300 gas utility and transport vehicles because a fuel vent may leak fuel, posing a fire hazard. No injuries have been reported.

    Product
    Club Car Gas Carryall 300, Transporter, Villager Vehicles, Streetrod Lux and Streetrod Vintage Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V608000·2019-08-19

    Horton Emergency Vehicles Recalled for Air Bag Cushion Defect

    Halcore Group is recalling 2018-2020 Horton Type I and III emergency vehicles because air bag cushions may detach and fail to inflate during a crash.

    Product
    HORTON — HORTON TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19770·2019-08-19

    Club Car Recalls Gas Golf Vehicles Due to Fire and Burn Hazards

    Club Car is recalling about 9,000 gas-powered golf and transport vehicles because a fuel line may leak, posing fire and burn hazards.

    Product
    Club Car Precedent, Tempo, Onward and Villager model gas golf and transport vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V604000·2019-08-16

    Forest River Recalls 2019 Rockport Vans Due to Welding Defect

    Forest River is recalling 2019 Rockport box vans and service bodies because improperly welded bulk storage beams may fail when loaded, posing an injury risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V605000·2019-08-16

    Mercedes-Benz Recalls 2019 CLS 450 for Electrical Wiring Defect

    Mercedes-Benz is recalling 2019 CLS 450 vehicles because an electrical line may chafe, causing engine stalls or electrical system failures that increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V603000·2019-08-15

    Land Rover Recalls 2018 Range Rovers for Backup Camera Software Defect

    Jaguar Land Rover is recalling 2018 Range Rover and Range Rover Sport vehicles because the backup camera may fail to display the rearview image, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2155-2019·2019-08-14

    SenTec Membrane Changer Set Recalled for Potential Electrolyte Application Failure

    SenTec AG is recalling 3 sets of Membrane Changer Sets because there is a 5% chance of insufficient electrolyte application during sensor changes.

    Product
    SenTec Membrane Changer Set (1 charger plus 1 insert) - Product Usage: is indicated for continuous, non-invasive monitoring of carbon dioxide tension and oxygen tension as well as oxygen saturation and pulse rate in adult and pediatric patients. In neonatal patients the SDMS is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2106-2019·2019-08-14

    Comet Technologies Recalls YXLON Cougar Cabinet X-Ray Systems

    Comet Technologies is recalling 93 YXLON Cougar Cabinet X-Ray Systems because the door interlocks fail to meet federal performance standards for power disconnection.

    Product
    YXLON Cougar Cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2137-2019·2019-08-14

    MED-EL SONATAti100 Cochlear Implant Recall for Leak Test Failures

    MED-EL is recalling 10 SONATAti100 cochlear implants because they failed helium-fine leak tests. The devices were distributed despite not meeting specifications.

    Product
    MED EL Cochlear Implant System, SONATATIi100, sold under the following implant types: a. SONATAti100 FLEXsoft; b. SONATAti100 H Standard; c. SONATAti100 Standard Product Usage: The SONATATIi100 Implant is an implantable part of the MED EL Cochlear Implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2220-2019·2019-08-14

    ROi Recalls Custom Surgical Packs Containing Stryker Pneumosure Tubesets

    ROi Consolidated Service Center is recalling 261 custom surgical packs containing Stryker Pneumosure tubesets that may detach from the cassette, potentially causing gas leaks.

    Product
    Regard ¿ custom surgical pack labeled as "LAP - FLOL LADY OF ANGELS" including recalled Stryker part numbers 0620 040 660 Pneumosure High Flow II Tubeset, 0620 040 690 Pneumosure Heated Tubeset with RTP and 0620 040 680 Pneumosure High Flow Tubeset with RTP.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2093-2019·2019-08-14

    Gk Photonics Atom Laser Projection Series Recalled for Safety Compliance

    Gk Photonics Inc is recalling the Atom Laser Projection Series because the provided remote interlock dongle does not fully comply with FDA manual reset requirements, posing a risk of high-power laser exposure.

    Product
    Atom Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2084-2019·2019-08-14

    Great Value Mild Taco Seasoning Recalled for Potential Salmonella Contamination

    CH Guenther & Sons, Inc. is recalling Great Value Mild Taco Seasoning because it contains cumin potentially contaminated with Salmonella.

    Product
    Great Value Mild Taco Seasoning, Net Wt. 1 OZ, Distributed by Wal-Mart Stores, Inc. Bentonville, AR. UPC 0 78742 24572v0
    Category
    Food
    Distribution
    27 states
  • HighFDA (Food)·F-1986-2019·2019-08-14

    Milkweed & Monarch Recalls Herbal Teas Due to Salmonella Risk

    Milkweed & Monarch, LLC is recalling specific lots of Ginger Spice, Sandia Rose, and Honey Lavender herbal teas due to potential Salmonella contamination.

    Product
    Sandia Rose, 1 oz (28.4 g), 2 oz, 4 oz, and 1-3 lb packages. An herbal tea, Taos, NM
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2097-2019·2019-08-14

    Gk Photonics Recalls Burstberry Laser Projection Series for Safety Defect

    Gk Photonics Inc is recalling the Burstberry Laser Projection Series because the provided remote interlock dongle fails to meet FDA safety requirements, posing a risk of high-power laser radiation exposure.

    Product
    Burstberry Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states