Go Backs

Surgical Equipment

AllImplants & Prosthetics(230)Monitoring Devices(252)Diagnostic Equipment(818)Home Healthcare(215)Contact Lenses & Vision(17)Surgical Equipment(896)

896 recalls

per page
Straumann USA
Medium RiskFDA Device

Straumann TLX/TLC SP Guided Implant Drivers Recalled for Missing Depth Markings

  • Sold in 4 states
  • Sold at Straumann USA LLC
Recalled
Added
Folsom Metal Products
Medium RiskFDA Device

DKS Disposable Kerrison Systems Recalled for Inadvertent Distribution

  • Sold in 5 states
  • Sold at Hospital distributors, Medical supply channels
Recalled
Added
Medium RiskFDA Device

Olympus Cystoscope Outer Sheath Recalled for Tip Damage and Incompatibility

  • Distributed nationwide
  • Sold at authorized medical distributors, direct sales
Recalled
Added
Megadyne Medical Products, Inc.: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode Recalled for Burn Risk
Critical RiskFDA Device

Megadyne Medical Products, Inc.: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode Recalled for Burn Risk

  • Distributed nationwide
  • Sold at hospitals, surgical centers +1 more
  • Reports of patient burns
Recalled
Added
Boston Scientific
Medium RiskFDA Device

Boston Scientific Corporation: iSLEEVE Expandable Introducer Set Recalled for Hemostatic Valve Leaks

  • Distributed nationwide
  • Sold at Authorized medical distributors, Direct sales to hospitals
  • Complaints associated with hemostatic valve leaks reported; no specific injury counts provided.
Recalled
Added
Medium RiskFDA Device

COR Disposable Kit Recalled Due to Missing Graft Loader Component Pin

  • Distributed nationwide
  • Sold at Hospitals, Medical device distributors
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon Research, LLC: Custom Surgical Procedure Packs Recalled for Mislabeled Latex-Free Status

  • Sold in Virginia
  • Sold at N VIRGINIA EYE SURG CTR
  • Undeclared latex
Recalled
Added
Bard Peripheral Vascular
Medium RiskFDA Device

Venclose digiRF Generators Recalled for Software-Induced Catheter Failure

  • Sold in 44 states
  • Sold at Hospital supply distributors, Direct medical sales
Recalled
Added
Karl Storz Endoscopy
Medium RiskFDA Device

Karl Storz Surgical Cutters, Resectors, and Burrs Recalled for Sterility Risks

  • Sold in 15 states
  • Sold at Direct medical supply channels
  • Environmental microorganisms due to loss of sterility contamination
Recalled
Added
B. Braun Medical
Medium RiskFDA Device

B. Braun Combined Spinal/Epidural Trays Recalled for Incorrect Connectors

  • Sold in Missouri, Oklahoma
  • Sold at Healthcare facilities, Medical distributors
Recalled
Added
MICROspecialties
Medium RiskFDA Device

MICROspecialties, Inc.: Injection Kits Recalled for Potential Sterilization Failure and Infection Risk

  • Sold in Missouri
Recalled
Added
Westmed
Critical RiskFDA Device

Westmed Flex Extenders Recalled for Life-Threatening Disconnection Risk

  • Sold in 30 states
  • Sold at Medical device distributors, Hospitals
  • 50,050 units affected
Recalled
Added
Maquet Medical Systems USA
Medium RiskFDA Device

Maquet Medical Systems USA: RotaFlow Centrifugal Pumps Recalled for Potential Sterile Barrier Breach

  • Sold in 12 states
  • Sold at Maquet Medical Systems USA, Hospital supply distributors
  • Pathogenic agents contamination
Recalled
Added
Intuitive Surgical
High RiskFDA Device

Intuitive Surgical, Inc.: da Vinci SP Surgical Patient Cart Recalled Due to Weak Belt Welds

  • Sold in 21 states
  • Sold at Intuitive Surgical, Inc., Hospital suppliers
Recalled
Added
Micro Therapeutics
Medium RiskFDA Device

Micro Therapeutics, Inc.: Apollo Onyx Delivery Microcatheters Recalled for Incorrect Instructions

  • Sold in 30 states
  • Sold at Authorized Medical Distributors
Recalled
Added
Medium RiskFDA Device

3M Company - Health Care Business: 3M Surgical Clipper Blades Recalled for Potential Burn Risk

  • Distributed nationwide
  • Sold at Worldwide distribution
  • Potential for minor injury/burns mentioned; no specific count of injuries provided.
Recalled
Added
Brasseler USA I
Medium RiskFDA Device

Brasseler USA I Lp: Super-Sharp Round Carbide Dental Burs Recalled Due to Latching Failure

  • Sold in 12 states
  • Sold at Direct distribution, Dental supply distributors
Recalled
Added
Steris
Medium RiskFDA Device

Steris Corporation: Steris Hookup Accessories Recalled Due to Illegible Identification Labels

  • Distributed nationwide
  • Sold at Steris Corporation, Authorized Medical Distributors
Recalled
Added
Cordis US
Critical RiskFDA Device

Cordis US Corp: Angiographic Catheterization Sets Recalled for Loss of Sterility

  • Sold in Oklahoma
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

Intuitive Da Vinci 5 Surgical System Recalled for User Interface Error

  • Sold in 6 states
  • Sold at Intuitive Surgical, Inc.
Recalled
Added
Intersurgical
Medium RiskFDA Device

Intersurgical Guedel Airway Devices Recalled for Plastic Burr Inhalation Risk

  • Sold in 10 states
  • Sold at Authorized medical distributors
  • Plastic burrs contamination
Recalled
Added
Angiodynamics
Medium RiskFDA Device

IsoLoc Prostate Immobilization Balloon Kits Recalled for Mislabeling

  • Sold in 7 states
  • Sold at Angiodynamics, Inc.
Recalled
Added
SEASPINE ORTHOPEDICS
Medium RiskFDA Device

NorthStar OCT Navigation Instruments Recalled for Misidentified Compatibility

  • Sold in 24 states
  • Sold at Authorized Medical Device Distributors, SeaSpine Direct Sales
Recalled
Added
Stryker Neurovascular
Medium RiskFDA Device

Stryker Trevo Trak 21 Microcatheters Recalled for Incorrect Labeling

  • Sold in California, Virginia
  • Sold at Stryker Neurovascular
Recalled
Added