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Surgical Equipment

AllImplants & Prosthetics(228)Monitoring Devices(259)Diagnostic Equipment(818)Home Healthcare(219)Contact Lenses & Vision(17)Surgical Equipment(898)

898 recalls

per page
Zimmer Surgical
Medium RiskFDA Device

Zimmer Surgical Inc: Zimmer Dermatome Blades Recalled for Uneven Thinness and Poor Graft Quality

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers +1 more
  • Issue identified at time of use; results in need for additional harvests to cover graft areas.
Recalled
Added
Medtronic Perfusion Systems
Medium RiskFDA Device

Medtronic Aortic Root Cannulas Recalled for Potential Sterility Breach

  • Sold in 7 states
  • Sold at Hospitals, Surgical centers
Recalled
Added
Stryker Spine
Medium RiskFDA Device

Stryker Spine: LITe Decompression Snake Arm Recalled for Incorrect Clamp Component

  • Sold in 4 states
  • Sold at Authorized medical distributors
Recalled
Added
Medium RiskFDA Device

Fortress Introducer Sheath System Recalled for Incorrect Size Labeling

  • Sold in 15 states
  • Sold at Hospitals, Medical distributors
Recalled
Added
Covidien: McGRATH MAC Video Laryngoscopes Recalled Due to Defective Stolen Units
Critical RiskFDA Device

Covidien: McGRATH MAC Video Laryngoscopes Recalled Due to Defective Stolen Units

  • Distributed nationwide
  • Sold at Unknown
Recalled
Added
Technicality
Medium RiskFDA Device

Technicality Inc.: Trumpet Needle Guide Recalled for Potential Ring Detachment and Injury Risk

  • Sold in Illinois
  • Sold at Technicality Inc.
  • 20,000 units affected
Recalled
Added
Medium RiskFDA Device

Vial2Bag Advanced Admixture Devices Recalled for Sterile Barrier Breach

  • Sold in 33 states
  • Sold at Progressive Medical Inc. (PMI), Hospitals
  • 129,600 units affected
Recalled
Added
Cook Vandergrift
Medium RiskFDA Device

Cook Vandergrift, Inc.: Cook Lead Clipper Recalled Due to Potential Loss of Packaging Sterility

  • Distributed nationwide
  • Sold at Hospital supply channels, Medical device distributors
  • 15,951 units affected
Recalled
Added
Nipro Medical
Medium RiskFDA Device

Surdial DX Hemodialysis Systems Recalled for Loose or Falling Screws

  • Sold in 21 states
  • Sold at Authorized medical device distributors, Specialty medical retailers
Recalled
Added
ETHICON
Medium RiskFDA Device

MONOCRYL Sutures Recalled for Incorrect Needle Size and Suture Length

  • Sold in 45 states
  • Sold at Authorized distributors, Medical supply channels
  • 16,524 units affected
Recalled
Added
Alcon Research
Critical RiskFDA Device

Alcon Custom Pak Procedure Packs Recalled for Incomplete Seals

  • Sold in California, North Dakota, Utah
  • Sold at Hospitals, Ophthalmic surgical centers +1 more
Recalled
Added
Integrity Implants
Medium RiskFDA Device

Repeater Bone Tamp Recalled for Incompatibility with Bone Funnels

  • Sold in 9 states
  • Sold at Integrity Implants Inc.
Recalled
Added
Medtronic Navigation
Critical RiskFDA Device

Medtronic Navigation, Inc.: StealthStation S8 Software Recalled for Surgical Planning Data Shifting

  • Sold in 51 states
  • Sold at Authorized Medical Distributors
Recalled
Added
Channel Medsystems
Medium RiskFDA Device

Cerene Cryotherapy Device Recalled for Nitrous Oxide Leakage Risk

  • Sold in 22 states
  • Sold at Healthcare facilities
Recalled
Added
Bard Peripheral Vascular
High RiskFDA Device

Bard Peripheral Vascular Inc: Magnum Disposable Tissue Biopsy Needles Recalled for Compromised Sterile Barrier

  • Distributed nationwide
  • Sold at Hospital supply distributors, Medical device distributors
Recalled
Added
INCIPIO DEVICES
Medium RiskFDA Device

Incipio Devices Offset Cup Impactors Recalled for Weld Fracture Risk

  • Sold in Tennessee
  • Sold at Medical distributors, Direct to hospitals
  • Incidents of fracture of the TIG weld reported; specific injury count not provided.
Recalled
Added
Cook
Medium RiskFDA Device

Cook Approach CTO Micro Wire Guides Recalled for Incorrect Expiration Dates

  • Sold at Specialized medical distributors
Recalled
Added
Baxter Healthcare
High RiskFDA Device

Baxter Healthcare Corporation: Boot Assembly Recalled for Detachment Risk and Potential Surgical Delay

  • Sold in Alabama
  • Sold at Baxter Healthcare Corporation
  • 1 customer report of the boot detaching from the traction system; no specific injury counts provided.
Recalled
Added
Augmedics
Medium RiskFDA Device

Augmedics Perc Pin Adaptor Recalled for Marking and Knob Defects

  • Distributed nationwide
  • Sold at surgical equipment distributors, hospitals
Recalled
Added
Medium RiskFDA Device

Medline Endo Kits Recalled for Missing Sterility and Expiration Labels

  • Sold in New York
  • Sold at Medical distributors, Healthcare facilities
Recalled
Added
Covidien
Medium RiskFDA Device

Covidien, LP: Tri-Staple 2.0 Intelligent Reloads Recalled for Potential Cartridge Damage

  • Distributed nationwide
  • Sold at Authorized medical distributors, Specialty healthcare providers
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Sterile Basic Eye Packs Recalled for Open Packaging Seals

  • Sold in Missouri
  • Sold at Medical supply distributors
Recalled
Added
Maquet Cardiovascular
Critical RiskFDA Device

Maquet VasoView Harvesting Systems Recalled for Wire and Silicone Defects

  • Distributed nationwide
  • Sold at Authorized medical distributors, Direct hospital sales
  • 429,177 units affected
Recalled
Added
Boston Scientific
Critical RiskFDA Device

Boston Scientific Corporation: POLARSHEATH Steerable Sheath Recalled for Potential Device Delamination

  • Distributed nationwide
  • Sold at Hospitals, Medical Supply Distributors
  • Device fragments contamination
Recalled
Added