Go Backs

Surgical Equipment

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

895 recalls

per page
Getinge Usa Sales
Medium RiskFDA Device

Getinge Usa Sales Inc: Meera Mobile Operating Table Recalled for Unintended Movement Risk

  • Distributed nationwide
  • Sold at Authorized Getinge medical equipment distributors, Direct sales to hospitals and surgical centers
Recalled
Added
Steris
Medium RiskFDA Device

Steris Corporation: Bandage Scissors Recalled Due to Potential Dye Residue Contamination

  • Distributed nationwide
  • Sold at medical distributors
  • Pink dye/residue contamination
Recalled
Added
Drs Vascular
Medium RiskFDA Device

Q-Stop Suture Retention Device Recalled for Performance Issues

  • Sold in Arkansas, California, New York
  • Sold at Drs Vascular, Inc.
Recalled
Added
Medtronic Perfusion Systems
Medium RiskFDA Device

Medtronic Affinity NT Oxygenator Recalled for Decreased CO2 Transfer Rates

  • Sold in Arizona, California, Tennessee
  • Sold at Hospital supply chains, Medical device distributors
Recalled
Added
Spectranetics
Medium RiskFDA Device

Spectranetics Corporation: Turbo-Elite Laser Catheters Recalled for Incorrect Product Labeling

  • Sold in 32 states
  • Sold at Hospitals, Medical facilities +1 more
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

da Vinci Surgical Systems Recalled for Software Error and Arm Fatigue

  • Sold in 30 states
  • Sold at Intuitive Surgical, Inc., Authorized Medical Device Distributors
Recalled
Added
TAS Medical
Medium RiskFDA Device

TAS Medical Tissue Approximation Systems Recalled for Breaking Straps

  • Sold in Louisiana, Oklahoma, Tennessee
  • Sold at Hospitals, Surgical centers
Recalled
Added
Wilson-Cook Medical
Medium RiskFDA Device

Cook Medical Hemospray Endoscopic Hemostat Recalled for Breaking Activation Knob

  • Sold at Medical distributors
Recalled
Added
Medium RiskFDA Device

Olympus ShockPulse-SE Lithotripsy System Recalled for Mis-wired Component

  • Distributed nationwide
  • Sold at Authorized Medical Distributors
Recalled
Added
LivaNova Deutschland
High RiskFDA Device

LivaNova Essenz Heart-Lung Machine Recalled for Touchscreen Display Failures

  • Sold in 9 states
  • Sold at LivaNova authorized distributors
Recalled
Added
Avanos Medical
Medium RiskFDA Device

Avanos Medical, Inc.: BALLARD Closed Suction Systems Recalled for Unlabeled DEHP Phthalate Content

  • Distributed nationwide
  • Sold at Medical distributors, Hospitals
  • Di(2-ethylhexyl) phthalate (DEHP) contamination
Recalled
Added
Karl Storz Endoscopy
Medium RiskFDA Device

Karl Storz Optical Biopsy and Grasping Forceps Recalled for Sterility Risk

  • Sold in 32 states
  • Sold at Authorized medical distributors, Direct hospital sales
Recalled
Added
Hologic
Medium RiskFDA Device

Sertera Biopsy Devices Recalled for Needle Separation and Dislodgement Risk

  • Distributed nationwide
  • Sold at Hospitals, Medical supply distributors +1 more
  • 55,335 units affected
Recalled
Added
OrganOx
High RiskFDA Device

OrganOx metra Perfusion System Recalled for Battery Short Circuit Risk

  • Sold in 11 states
  • Sold at Specialty medical distributors, OrganOx Ltd
Recalled
Added
MICROVENTION
Medium RiskFDA Device

LIFEPEARL Drug Elutable Microspheres Recalled for Undersized Diameter

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

HARMONIC FOCUS Shears Recalled for Continuous Activation Risk

  • Distributed nationwide
  • Sold at Surgical centers, Medical facilities +1 more
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon Custom Pak Surgical Packs Recalled for Incorrect Latex-Free Labeling

  • Sold in 13 states
  • Sold at Hospitals, Surgical centers
Recalled
Added
Medtronic Neuromodulation
Medium RiskFDA Device

Medtronic Neuromodulation: Vanta Implantable Neurostimulator Recalled for Premature Battery Depletion

  • Distributed nationwide
  • Sold at authorized healthcare providers
  • Premature battery life depletion leading to outpatient reprogramming or earlier than anticipated surgical replacements.
Recalled
Added
American Contract Systems
Medium RiskFDA Device

Lower Extremity and Total Knee Packs Recalled for Chemical Residue

  • Sold in Colorado
  • Sold at American Contract Systems, Inc.
  • Ethylene Oxide, Ethylene Chlorohydrin contamination
Recalled
Added
Ethicon
Medium RiskFDA Device

Ethicon, Inc.: STRATAFIX Spiral MONOCRYL Plus Suture Devices Recalled for Compromised Sterility

  • Sold in 9 states
  • Sold at Ethicon, Inc. Authorized Distributors
Recalled
Added
Medium RiskFDA Device

Olympus LithoCrushV Mechanical Lithotriptors Recalled for Distal Tip Tearing

  • Distributed nationwide
  • Sold at Authorized medical distributors
Recalled
Added
Calyxo
Critical RiskFDA Device

Calyxo CVAC Aspiration System Recalled for Excessive Intrarenal Pressure Risk

  • Sold in 41 states
  • Sold at Direct to hospitals, Specialized medical distributors
  • 11,246 units affected
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: Roller Bar Electrodes Recalled for Incorrect Pouch Labeling

  • Sold in 13 states
  • Sold at Authorized medical distributors
Recalled
Added
Alcon Research
Low RiskFDA Device

Alcon Custom-Pak Surgical Kits Recalled for Tubing Valve Breakage

  • Sold in Delaware, Illinois, Oklahoma
  • Sold at Christiana Care Health Services, Mercy Hospital +2 more
Recalled
Added