Go Backs

Surgical Equipment

AllImplants & Prosthetics(225)Monitoring Devices(272)Diagnostic Equipment(819)Home Healthcare(232)Contact Lenses & Vision(17)Surgical Equipment(890)

890 recalls

per page
AVID Medical
Critical RiskFDA Device

Halyard and Cardiac Cath Kits Recalled for Syringe Disconnection Risk

  • Sold in 7 states
  • Sold at Hospitals, Surgical Centers +1 more
  • 19,413 units affected
Recalled
Added
Erbe Medical
Medium RiskFDA Device

Erbe Medical ERBEFLO CleverCap and Tubing Recalled for Aspiration Risk

  • Sold in 52 states
  • Sold at Authorized Medical Distributors, Direct Sales to Hospitals/Clinics
  • 289,821 units affected
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

da Vinci X and Xi Surgical Systems Recalled for Breaking Arm Screws

  • Sold in 49 states
  • Sold at Direct Sales, Hospital Distributors
Recalled
Added
Intuitive Surgical
Critical RiskFDA Device

Intuitive 8 mm SureForm 30 Gray Reloads Recalled for Incomplete Staple Line

  • Sold in 49 states
  • Sold at Hospitals, Surgical Centers
Recalled
Added
Merit Medical Systems
Medium RiskFDA Device

Philips Bridge Prep Kit Recalled for Catheter Advancement Issues

  • Sold in Colorado
  • Sold at Medical distributors
Recalled
Added
Elekta
Medium RiskFDA Device

Leksell Vantage Arc System Recalled for Potential Coordinate Shifting

  • Sold in 32 states
  • Sold at Elekta, Inc. Authorized Distributors
Recalled
Added
Zimmer
Medium RiskFDA Device

Disposable Mixing Bowls and Spatulas Recalled for Defective Package Seals

  • Sold in 31 states
  • Sold at Hospital suppliers, Medical device distributors
  • Ten complaints received regarding package seal issues; no specific injury counts provided.
Recalled
Added
Medtronic
High RiskFDA Device

Medtronic Sphere-9 Catheter Recalled Due to Heart Rhythm Interactions

  • Distributed nationwide
  • Sold at medical supply distributors, hospitals +1 more
  • Observations of ventricular fibrillation (VF) during therapy.
Recalled
Added
Healthmark Industries
Medium RiskFDA Device

Mesh Style Tip Protectors Recalled for Lack of FDA Clearance

  • Distributed nationwide
  • Sold at Authorized distributors, Direct sales
  • 4,291,797 units affected
Recalled
Added
Clinical Innovations
Medium RiskFDA Device

Kiwi Omni Vacuum Delivery System Recalled for Device Breakage Risk

  • Sold in 37 states
  • Sold at Hospital suppliers, Medical distributors
  • Complaints of device breakage; no specific injury counts provided.
Recalled
Added
Diversatek Healthcare
Medium RiskFDA Device

Diversatek Viper 3-Stage Balloon Dilators Recalled for Incorrect Pressure Labels

  • Sold in 19 states
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
Windstone Medical Packaging
Medium RiskFDA Device

Custom Convenience Kits Pre Op Kits Recalled for IV Set Backflow Risk

  • Sold in 4 states
  • Sold at Hospitals, Surgical centers +1 more
Recalled
Added
LSL Healthcare
Medium RiskFDA Device

LSL Healthcare Medical Procedure Kits Recalled for Non-Sterile Alcohol Pads

  • Sold in Maryland, Illinois, Minnesota
  • Sold at LSL Healthcare Inc.
  • Non-sterile microbes contamination
Recalled
Added
ARROW INTERNATIONAL
Medium RiskFDA Device

Arrow Catheter Kits and Needles Recalled for Defective Liquid Adhesive

  • Sold in 9 states
  • Sold at Direct medical distribution, Hospitals +1 more
Recalled
Added
SurgiSmoke Solutions
Medium RiskFDA Device

Flamingo Funnel Medical Devices Recalled for Sterilization Issues

  • Sold in 13 states
  • Sold at Hospital supply chains, Medical device distributors
Recalled
Added
Medium RiskFDA Device

Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes Recalled

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Olympus Direct Sales
  • 48,999 units affected
Recalled
Added
XTANT Medical
Medium RiskFDA Device

nanOss 3D Bone Graft Substitutes Recalled for Incorrect Shelf Life

  • Sold in 9 states
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
Davol
Medium RiskFDA Device

Avitene Ultrafoam Hemostat Recalled for Insect Fragment Contamination

  • Distributed nationwide
  • Sold at hospitals, healthcare facilities
  • Insect fragments contamination
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Convenience Kits Recalled for Unapproved Design Changes

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Direct Sales to Hospitals
  • 270,311 units affected
Recalled
Added
Medline Industries
Medium RiskFDA Device

Namic and Medline Guidewires and Syringes Recalled for Regulatory Issues

  • Distributed nationwide
  • Sold at specialty medical distributors, hospitals +2 more
  • 629,606 units affected
Recalled
Added
Medium RiskFDA Device

Olympus Thunderbeat II Shears Recalled for Distal Tip Detachment Risk

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas, Medical distributors
Recalled
Added
Medium RiskFDA Device

Integra CUSA Clarity C7000 Console Recalled for Unresponsive Touch Screen

  • Sold in Michigan, New York
  • Sold at Authorized Medical Distributors, Direct Hospital Sales
Recalled
Added
Medline Industries
High RiskFDA Device

Centurion Circumcision Kits Recalled for Lack of Sterility

  • Sold in South Carolina
  • Sold at Nationwide distribution
  • Non-sterile medical device contamination
Recalled
Added
Medium RiskFDA Device

Cytal Wound and Burn Matrix Recalled for High Endotoxin Levels

  • Sold in 32 states
  • Sold at Authorized Medical Distributors, Hospitals +1 more
  • Endotoxins contamination
Recalled
Added