Go Backs

Medical Devices

Medical Devices product recalls

AllImplants & Prosthetics(226)Monitoring Devices(263)Diagnostic Equipment(818)Home Healthcare(223)Contact Lenses & Vision(17)Surgical Equipment(895)

2,692 recalls

per page
Getinge Usa Sales
Medium RiskFDA Device

MEERA Mobile Operating Tables Recalled Due to Hand Control Movement Errors

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Getinge Direct Sales
Recalled
Added
Medium RiskFDA Device

MEDLINE INDUSTRIES, LP - Northfield: Medline Surgical Kits Recalled for Incorrectly Labeled Vessel Cannulae

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
Medium RiskFDA Device

Medline Surgical Instruments Recalled for Compromised Sterility Risk

  • Distributed nationwide
  • Sold at Medline Industries, Medical distributors +2 more
  • 21,440 units affected
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon Research LLC: ClearCut and A-OK Ophthalmic Knives Recalled for Reduced Sharpness

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Specialty Ophthalmic Suppliers
  • Increase in complaint reports related to sharpness detected; specific injury counts not provided in the alert text.
Recalled
Added
Philips Respironics
Critical RiskFDA Device

Philips Respironics, Inc.: Trilogy and Garbin EVO Ventilators Recalled for Sudden Loss of Ventilation

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Specialty Retailers +1 more
  • 146,523 units affected
Recalled
Added
Biomet
Medium RiskFDA Device

Biomet, Inc.: Biomet Compress Device Anchor Plugs Recalled for Potential Metal Burrs

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Hospitals +1 more
  • Metal burrs contamination
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips North America Llc: Magnetic Resonance Systems Recalled for Incorrect Support Table Installation

  • Distributed nationwide
  • Sold at Philips authorized medical equipment distributors, specialized hospital supply chains
  • 10,221 units affected
Recalled
Added
Smiths Medical ASD
Critical RiskFDA Device

Smiths Medical ASD Inc.: Bivona Tracheostomy Silicone Tubes Recalled for Securement Flange Tearing

  • Distributed nationwide
  • Sold at specialty medical suppliers, authorized medical device distributors
  • 241,980 units affected
Recalled
Added
Maquet Cardiovascular
Medium RiskFDA Device

Maquet Cardiovascular, LLC: Vasoview Hemopro Endoscopic Vessel Harvesting Systems Recalled for Debris Risk

  • Distributed nationwide
  • Sold at hospitals, surgical centers +1 more
  • Polyimide particulate matter contamination
Recalled
Added
NOXBOX
Critical RiskFDA Device

NOxBOXi Nitric Oxide Delivery System Recalled for Dose Fluctuations

  • Sold in Tennessee
  • Sold at Linde, NBL
Recalled
Added
Covidien
Medium RiskFDA Device

Covidien, LP: Structural Balloon and Blunt Tip Trocars Recalled for Seal Disengagement

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Hospitals +1 more
  • 774,229 units affected
Recalled
Added
Fresenius Medical Care
Critical RiskFDA Device

Fresenius Medical Care Holdings, Inc.: stay-safe Catheter Extensions and Adapters Recalled for Tubing Contamination

  • Distributed nationwide
  • Sold at Fresenius Medical Care Holdings, Inc., Medical distributors
  • NDL PCBAs contamination
Recalled
Added
Boston Scientific
High RiskFDA Device

Boston Scientific Corporation: EndoVive PEG Feeding Tube Kits Recalled for Blocked Barb Connector

  • Distributed nationwide
  • Sold at Boston Scientific Corporation, Medical Supply Distributors
Recalled
Added
AVID Medical
Medium RiskFDA Device

CLEARIFY Visualization System Recalled for Discoloration from Resterilization

  • Sold in 7 states
  • Sold at Medical facilities, Specialized surgical centers
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon PRECISION1 One-Day Contact Lenses Recalled for Weak Seal and Sterility Risk

  • Sold in 19 states
  • Sold at Authorized eye care providers
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips Microstream CO2 Filter Lines Recalled for Disconnection Issues

  • Distributed nationwide
  • Sold at Hospital supply distributors, Medical device retailers
  • 486,631 units affected
Recalled
Added
Medium RiskFDA Device

Philips Medical Systems Quadrature Body Coils Recalled for Loose Seals

  • Distributed nationwide
  • Sold at Medical facilities, Authorized Philips medical distributors
Recalled
Added
Medium RiskFDA Device

Medline Medical Convenience Kits Recalled for Syringe Quality Issues

  • Distributed nationwide
  • Sold at specialty medical distributors, hospitals +1 more
  • 50,482 units affected
Recalled
Added
LEICA BIOSYSTEMS NUSSLOCH
Medium RiskFDA Device

LEICA BIOSYSTEMS NUSSLOCH GMBH: Cryostats Recalled Due to Fire and Burn Risk from Flammable Freezing Sprays

  • Distributed nationwide
  • Sold at Authorized medical device distributors, Direct sales from Leica Biosystems
Recalled
Added
Guangzhou Pluslife Biotech
Medium RiskFDA Device

MiniDock Devices and Pluslife COVID-19 Test Kits Recalled for Lacking FDA Clearance

  • Distributed nationwide
  • Sold at Authorized distributors
Recalled
Added
Fujirebio Diagnostics
Medium RiskFDA Device

Lumipulse Alzheimer's Test Kits Recalled for Inaccurate Results

  • Sold in 13 states
  • Sold at Clinical laboratories, Medical facilities
Recalled
Added
Medium RiskFDA Device

FLEX CD20cy (Dako Omnis) Antibody Recalled for Potential False Negative Risk

  • Sold in 32 states
  • Sold at Authorized medical laboratory distributors, Agilent Technologies
Recalled
Added
Baxter Healthcare
Critical RiskFDA Device

Welch Allyn and Breathe Technologies Life2000 Ventilators Recalled for Battery Failure

  • Distributed nationwide
  • Sold at authorized healthcare dealers, medical equipment suppliers
Recalled
Added
Tyber Medical
Medium RiskFDA Device

Tyber Medical A.L.P.S. mvX Plates Recalled for Screw Locking Failure

  • Distributed nationwide
  • Sold at authorized medical distributors
  • Surgical delays have been reported with the use of the devices due to screw-locking failure.
Recalled
Added