Go Backs

Surgical Equipment

AllImplants & Prosthetics(230)Monitoring Devices(252)Diagnostic Equipment(819)Home Healthcare(215)Contact Lenses & Vision(17)Surgical Equipment(896)

896 recalls

per page
Argon Medical Devices
Medium RiskFDA Device

Argon Medical Devices, Inc: L-CATH PICC Catheters Recalled for Incorrect Catheter Length in Package

  • Sold in 4 states
Recalled
Added
Medium RiskFDA Device

Medline Medical Convenience Kits Recalled for Syringe Leaks and Breakage

  • Distributed nationwide
  • Sold at Hospital supply chains, Medical distributors
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: InstaClear Lens Sheath Recalled for Potential to Break During Surgery

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas, Direct distribution to hospitals and clinics
Recalled
Added
Boston Scientific
Critical RiskFDA Device

Boston Scientific Carotid WALLSTENT Recalled for Delivery System Resistance

  • Distributed nationwide
  • Sold at Hospital supply distributors, Medical device wholesalers
  • Physicians encountered greater than anticipated resistance during withdrawal; most serious potential adverse consequence is stroke.
Recalled
Added
Tornier S.A.S.
Medium RiskFDA Device

Stryker Blueprint Mixed Reality Glenoid Pin Guide Recalled for Disassembly Risk

  • Sold in 7 states
  • Sold at Hospitals, Surgical Centers
Recalled
Added
Qapel Medical
Critical RiskFDA Device

Hippo 072 Aspiration Systems Recalled for Tip Detachment and Vessel Rupture

  • Sold in 29 states
  • Sold at Authorized Medical Distributors, Hospitals
Recalled
Added
Mazor Robotics
Medium RiskFDA Device

Mazor X Orthopedic Instrument Recalled for Software Display Anomalies

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Medtronic
Recalled
Added
Carbon Medical Technologies
Low RiskFDA Device

BiomarC EX Fiducial Marker System Recalled for Missing MRI Safety Inserts

  • Sold in Tennessee
  • Sold at authorized medical distributors
Recalled
Added
Auris Health
Medium RiskFDA Device

MONARCH Bronchoscopes Recalled for Potential Device Leaks

  • Sold in 31 states
  • Sold at Medical Facilities, Hospitals +1 more
Recalled
Added
BALT USA
Medium RiskFDA Device

Balt Optima and Prestige Coil Systems Recalled for Visibility Defect

  • Sold in 39 states
  • Sold at Hospitals, Medical centers +1 more
Recalled
Added
ARROW INTERNATIONAL
Critical RiskFDA Device

ARROW INTERNATIONAL Inc.: QuickFlash Radial Artery Catheterization Kits Recalled for Defective Guidewire

  • Distributed nationwide
  • Sold at hospitals, medical distributors
  • Reports received indicating resistance of the guidewire handle/chamber; potential for arterial vasospasm and vessel injury.
Recalled
Added
Smith & Nephew
Medium RiskFDA Device

Smith & Nephew K-Wires Recalled for Packaging and Sizing Error

  • Distributed nationwide
  • Sold at Hospital and surgical supply channels
Recalled
Added
Stryker
Medium RiskFDA Device

Stryker Guide Wire with Ruler Tube Recalled for Metal Ring Detachment Risk

  • Sold in 11 states
  • Sold at Hospitals, Surgical centers
  • Metal fragments contamination
Recalled
Added
MicroPort Orthopedics
Medium RiskFDA Device

MicroPort HIPTURN Femoral Head Trials Recalled for Missing FDA Authorization

  • Sold in 13 states
  • Sold at Medical device distributors
Recalled
Added
Medium RiskFDA Device

Centurion Sterile CirClamps Recalled for Packaging Holes and Sterility Loss

  • Distributed nationwide
  • Sold at Authorized medical distributors, Hospitals +1 more
  • 498,354 units affected
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: SOLTIVE SuperPulsed Laser Fibers Recalled for Breached Sterile Seals

  • Sold in 27 states
  • Sold at Authorized medical distributors
Recalled
Added
Thoratec
Medium RiskFDA Device

Thoratec Corp.: Heartmate LVAS Implant Kits and Coring Knives Recalled for Dullness

  • Sold in 41 states
  • Sold at Direct distribution to hospitals and medical facilities
Recalled
Added
Atrium Medical
High RiskFDA Device

Atrium Medical Corporation: Advanta V12 Covered Stent System Recalled for Potential Balloon Weld Failure

  • Sold at Hospitals, Medical distributors
Recalled
Added
Boston Scientific
Medium RiskFDA Device

Boston Scientific Extractor Pro RX Catheters Recalled for Labeling Error

  • Sold in 19 states
  • Sold at Medical distributors, Direct to hospitals
Recalled
Added
DeRoyal Industries
Medium RiskFDA Device

DeRoyal Industries Inc: Head and Neck Surgical Kits Recalled for Damaged Syringe Packaging

  • Sold in Pennsylvania
  • Sold at authorized distributors
Recalled
Added
Belmont Instrument
Medium RiskFDA Device

Allon 2001 Patient Wraps Recalled for Potential Overheating Risk

  • Sold in 9 states
  • Sold at Authorized Medical Distributors, Direct Hospital Sales
  • One report of the patient wrap exceeding set temperature; no specific injuries detailed.
Recalled
Added
Channel Medsystems
Medium RiskFDA Device

Channel Medsystems, Inc.: Cerene Cryotherapy Device Recalled for Incomplete Troubleshooting Instructions

  • Sold in 36 states
  • Sold at Healthcare facilities, Hospitals
Recalled
Added
Medium RiskFDA Device

Jewel Precision Sterilization Containers Recalled for Incorrect Instructions

  • Sold in Indiana, New York, Pennsylvania
  • Sold at specialty retailers
Recalled
Added
Medium RiskFDA Device

Medline Iris Scissors Recalled Due to Potential Loss of Sterility

  • Sold in 21 states
  • Sold at Medline Industries, Medical distributors
  • 69,611 units affected
Recalled
Added