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Other product recalls

AllMarine & Watercraft(7)Alcohol & Tobacco(10)Hazardous Materials(19)Industrial & Commercial(66)Uncategorized(12)

138 recalls

per page
Alliance Chemical 1-K Kerosene Heater Fuel Recalled for Flash Fire Risks
Critical RiskCPSC

Alliance Chemical 1-K Kerosene Heater Fuel Recalled for Flash Fire Risks

  • Distributed nationwide
  • Sold at Amazon.com, AllianceChemical.com
  • 30,155 units affected
Recalled
Added
mGanna Sodium Hydroxide Pellets Recalled for Burn and Irritation Risks
High RiskCPSC

mGanna Sodium Hydroxide Pellets Recalled for Burn and Irritation Risks

  • Distributed nationwide
  • Sold at Amazon.com, Archie Xpress
  • Sodium hydroxide contamination
Recalled
Added
Prestige Supernova and Typhoon Lighters Recalled for Fire and Burn Hazards
High RiskCPSC

Prestige Supernova and Typhoon Lighters Recalled for Fire and Burn Hazards

  • Distributed nationwide
  • Sold at Small independent stores, prestigeimportgroup.com
Recalled
Added
Medium RiskFDA Food

American Snuff Company, LLC - Memphis: Grizzly and Kodiak Snuff Products Recalled for Potential Plastic Contamination

  • Sold in 48 states
  • Sold at retail stores
  • Plastic fragments contamination
Recalled
Added
U.S. Smokeless Tobacco Mfg
Medium RiskFDA Food

U.S. Smokeless Tobacco Mfg Co. LLC: The discovery of a potential product incident associated with US Smokeless Tobacco Company LLC (USSTC) products involving a non-product related material.

  • Foreign material contamination
Recalled
Added
Drip More
Medium RiskFDA Food

Drip More LLC: Candy King Worms E-Liquid Recalled for High Nicotine Content

  • Sold in 26 states
  • Sold at wholesalers, distributors +1 more
  • Nicotine contamination
Recalled
Added
Kodiak Premium Wintergreen Longcut Tobacco Recalled for Foreign Metal Objects
Medium RiskFDA Food

Kodiak Premium Wintergreen Longcut Tobacco Recalled for Foreign Metal Objects

  • Sold in 18 states
  • Sold at Retailers
  • Metal fragments contamination
Recalled
Added
Jost Chemical
Medium RiskFDA Food

Jost Chemical Zinc Sulfate Monohydrate Powder Recalled for Elevated Lead

  • Sold in 4 states
  • Sold at Industrial distributors, Manufacturing suppliers
  • Lead contamination
Recalled
Added
Wedgewood Village Pharmacy
Medium RiskFDA Vet

Wedgewood Village Pharmacy, LLC: Insanitary conditions.

  • 190,408 units affected
Recalled
Added
Epilog Laser
High RiskFDA Device

Epilog Laser Corp.: Fusion Pro 24 Laser Systems Recalled for Radiation Exposure Risk

  • Distributed nationwide
  • Sold at authorized distributors
Recalled
Added
YAMAHA MOTOR
Medium RiskFDA Device

YAMAHA MOTOR CORPORATION: Industrial Surface Mounters and Inspection Systems for Missing Safety Labels

  • Distributed nationwide
  • Sold at Yamaha Motor Corporation
Recalled
Added
Trimble Ab
Medium RiskFDA Device

Trimble RTS873 Robotic Total Stations Recalled for Excessive Laser Power

  • Distributed nationwide
  • Sold at Specialty contractors, General contractors +1 more
Recalled
Added
Jinan Bodor Cnc Machine
Medium RiskFDA Device

Bodor I Series Laser Cutting Machines Recalled for Safety Standard Violations

  • Distributed nationwide
  • Sold at Authorized distributors
Recalled
Added
Apic Yamada America
Medium RiskFDA Device

Apic Yamada Molding Equipment Recalled for Missing FDA Compliance Labels

  • Distributed nationwide
  • Sold at Apic Yamada America
Recalled
Added
Jinan Bodor Cnc Machine
Medium RiskFDA Device

Bodor P and C Series Laser Cutting Machines Recalled for Laser Non-Compliance

  • Distributed nationwide
  • Sold at Authorized industrial equipment distributors
Recalled
Added
Medium RiskFDA Device

Atomstack Material Processing Laser Products Recalled for Safety Defect

  • Distributed nationwide
  • Sold at Authorized distributors
Recalled
Added
High RiskFDA Device

Rygel Advanced Machines d/b/a Omtech Laser: OMTech Desktop Laser Engravers Recalled for Laser Safety Violations

  • Distributed nationwide
  • Sold at Omtech Laser
Recalled
Added
Medtronic Neuromodulation
Medium RiskFDA Device

Medtronic Neuromodulation: Medtronic recently identified that if the SynchroMed II pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug delivery after leaving the MRI magnetic field, which is inconsistent with the current labeling.

  • 176,843 units affected
Recalled
Added
Exactech
Medium RiskFDA Device

Exactech, Inc.: The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).

  • 171,322 units affected
Recalled
Added
Abbott Medical
Critical RiskFDA Device

Abbott Medical: Firm has received complaints from patients who are unable to exit MRI (Magnetic Resonance Imaging) mode on their IPGs (Implantable Pulse Generators).

  • 197,879 units affected
Recalled
Added
CareFusion 303
Medium RiskFDA Device

CareFusion 303, Inc.: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

  • 510,075 units affected
Recalled
Added
Gilbarco
Medium RiskNHTSA

Gilbarco, Inc.: Orpak/Gasboy Automatic Tank Gauges Recalled for Fire Risk

  • Distributed nationwide
  • Sold at authorized dealers
  • 12,000 units affected
Recalled
Added
WHITE RIVER MARINE
Medium RiskNHTSA

2024-2025 Tracker Trailstar TRL and Topper Trailers Recalled for Winch Failure

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added
Medium RiskNHTSA

2024-2025 Skeeter FXR Boat Trailers Recalled for Ladder Weld Failure

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added