Go Backs

Surgical Equipment

AllImplants & Prosthetics(229)Monitoring Devices(257)Diagnostic Equipment(818)Home Healthcare(218)Contact Lenses & Vision(17)Surgical Equipment(896)

896 recalls

per page
Zimmer Surgical
Medium RiskFDA Device

Zimmer Air and AN Dermatomes Recalled for Misaligned Thickness Control Bar

  • Distributed nationwide
  • Sold at Zimmer Surgical Inc, Surgical equipment distributors +1 more
Recalled
Added
Medium RiskFDA Device

Canadian Hospital Specialties Ltd.: High Flow Insufflation Tubing Recalled for Compromised Sterility

  • Sold in Massachusetts
  • Sold at Hospital distributors, Medical supply channels
Recalled
Added
Encore Medical
Medium RiskFDA Device

DJO Surgical AltiVate Reamers Recalled for Potential to Kick or Bind Up

  • Sold in 27 states
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

Intuitive Surgical, Inc.: Da Vinci Single-Site Wristed Needle Driver Recalled for Uncontrollable Movement

  • Sold in 14 states
  • Sold at Intuitive Surgical, Inc.
Recalled
Added
Apellis Pharmaceuticals
Medium RiskFDA Device

Apellis Pharmaceuticals, Inc.: Apellis Injection Kits Recalled for Filter Needle Structural Variations

  • Distributed nationwide
  • Sold at Authorized medical distributors
  • Rare events of retinal vasculitis reported; causal relationship not established.
Recalled
Added
CooperSurgical
Medium RiskFDA Device

CooperSurgical, Inc.: Carter-Thomason CloseSure System XL Recalled for Incorrect Component Labels

  • Sold in Missouri
Recalled
Added
Critical RiskFDA Device

Olympus Forceps and Irrigation Plugs Recalled for Potential Contamination

  • Distributed nationwide
  • Sold at authorized medical distributors, Olympus Corporation of the Americas
  • biomaterial contamination
Recalled
Added
Medium RiskFDA Device

Medline General Surgery Trays Recalled for Hemorrhage Risk

  • Sold in 4 states
  • Sold at Hospital suppliers, Medical device distributors
Recalled
Added
Belmont Instrument
Medium RiskFDA Device

Belmont 3.0 Liter Disposable Sets for Rapid Infuser Recalled for Fluid Leaks

  • Sold in 33 states
  • Sold at Medical distributors, Direct to hospitals
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: SOLTIVE SuperPulsed Laser Fibers Recalled for Fiber Breakage Risk

  • Distributed nationwide
  • Sold at Authorized medical distributors
  • 82,200 units affected
Recalled
Added
Maquet Cardiovascular
Medium RiskFDA Device

Heartstring III Proximal Seal System Recalled for Potential Failure to Seal

  • Distributed nationwide
  • Sold at Medical device distributors, Direct surgical supply channels
  • 40,928 units affected
Recalled
Added
Medium RiskFDA Device

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.: Directional Laser Probes Recalled for Difficulty Retracting or Directing Tips

  • Sold in 11 states
  • Sold at Authorized medical distributors
Recalled
Added
Windstone Medical Packaging
Medium RiskFDA Device

Aligned Medical Convenience Kits Recalled for Defective Suction Tubes

  • Sold in 5 states
  • Sold at Clinical facilities, Hospitals
Recalled
Added
Angiodynamics
Medium RiskFDA Device

Angiodynamics, Inc.: Vascular Access Kits Recalled for Loose Metal Shavings and Embolism Risk

  • Sold in Virginia
  • Sold at Hospital supply networks, VA facilities
  • Metal shavings contamination
Recalled
Added
Howmedica Osteonics
Medium RiskFDA Device

Stryker CranialMask Tracker Recalled for Surgical Software Error

  • Distributed nationwide
  • Sold at Authorized medical distributors, Hospitals
Recalled
Added
Abiomed
Medium RiskFDA Device

Abiomed, Inc.: Impella Catheters Recalled for Updated Instructions Regarding Low Blood Flow

  • Distributed nationwide
  • Sold at Hospitals, Medical Specialty Retailers +1 more
  • Fibers contamination
Recalled
Added
Maquet Medical Systems USA
Medium RiskFDA Device

Maquet Medical Systems USA: HLS Set Advanced Emergency Priming Line Recalled for Sterile Barrier Defect

  • Distributed nationwide
  • Sold at Maquet Medical Systems USA
  • 16,520 units affected
Recalled
Added
LINK BIO
Medium RiskFDA Device

LINK BIO CORP: SymphoKnee Patella Sizing Template Recalled for Incorrect Labeling

  • Sold in 5 states
  • Sold at authorized distributors, medical facilities
Recalled
Added
Sklar Instruments
Medium RiskFDA Device

ECONO STERILE Medical Kits Recalled for Packaging and Sterility Breaches

  • Distributed nationwide
  • Sold at Medical distributors, Healthcare facilities +1 more
  • Potential microbial contamination due to breach of sterile barrier contamination
Recalled
Added
ICU Medical
Medium RiskFDA Device

ICU Medical ChemoLock and ChemosafeLock Devices Recalled for Potential Leaks

  • Sold in 38 states
  • Sold at Medical distributors, Hospitals +1 more
  • 789,239 units affected
Recalled
Added
Karl Storz Endoscopy
Medium RiskFDA Device

Karl Storz Endoscopy: Flexible Intubation Endoscopes Recalled Due to Sterility Assurance Issues

  • Sold in 46 states
  • Sold at Karl Storz Endoscopy
Recalled
Added
HUMAN MED AG
Medium RiskFDA Device

Biofill Infiltration Cannulas Recalled for Defective Spray Nozzle

  • Sold in Florida
  • Sold at authorized medical distributors
Recalled
Added
Medtronic Perfusion Systems
Critical RiskFDA Device

Medtronic Aortic Root Cannulae Recalled for Loose Material and Stroke Risk

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Direct Sales to Hospitals
  • Loose particulate material contamination
Recalled
Added
Merit Medical Systems
Medium RiskFDA Device

Merit Medical Monarch Inflation Devices Recalled for Sterile Barrier Defect

  • Sold in 46 states
  • Sold at Hospitals, Medical clinics +1 more
  • Environmental bacteria (due to sterile barrier breach) contamination
Recalled
Added