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
Microtek Medical
Medium RiskFDA Device

Microtek and Ecolab Patient Drapes Recalled for Incorrect Sterile Labeling

  • Sold in 20 states
  • Sold at Microtek Medical, Inc., Ecolab
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline IV Administration Kits Recalled for Defective Check Valves

  • Distributed nationwide
  • Sold at Medical supply distributors, Healthcare facilities +1 more
  • Customer complaints received regarding check valve components; no specific patient injuries enumerated in the provided record.
Recalled
Added
Cardinal Health 200
Medium RiskFDA Device

Cardinal Health Salem Sump Stomach Tubes Recalled for Valve Breakage Risk

  • Distributed nationwide
  • Sold at Hospitals, Medical supply distributors +2 more
  • Reports of breakage in the Anti-Reflux Valve (ARV) were received; specific injury counts not provided.
Recalled
Added
Medium RiskFDA Device

Siemens Medical Solutions USA, Inc: Cios Mobile X-ray Systems Recalled Due to Software Issue and Potential Misdiagnosis

  • Distributed nationwide
  • Sold at Authorized medical device distributors, Direct sales to hospitals and surgical centers
Recalled
Added
Medium RiskFDA Device

Proxima Sterile Surgical Drapes Recalled for Potential Sterility Loss

  • Distributed nationwide
  • Sold at Medline Industries, LP, Authorized medical supply distributors
Recalled
Added
Medium RiskFDA Device

Vercise Deep Brain Stimulation Burr Hole Cover Kits Recalled for Locking Defect

  • Sold in 45 states
  • Sold at Medical device distributors, Surgical centers +1 more
  • 24,583 units affected
Recalled
Added
Zap Surgical Systems
Medium RiskFDA Device

ZAP-X Radiosurgery Systems Recalled for Collision Risk Due to Software Defect

  • Sold in 4 states
  • Sold at Authorized medical device distributors, Zap Surgical Systems direct sales
Recalled
Added
Medium RiskFDA Device

Medical Action Industries, Inc. 306: IV Start Kits Recalled Due to Compromised Saline Flush Syringes

  • Sold in Minnesota, North Dakota
  • 206,200 units affected
Recalled
Added
Stryker
Medium RiskFDA Device

Stryker Neuro Match Heads Recalled for Potential Packaging and Labeling Errors

  • Distributed nationwide
  • Sold at authorized medical distributors, hospital procurement channels
Recalled
Added
Aesculap
Medium RiskFDA Device

Aesculap Forceps Recalled Due to Risk of Breakage During Use

  • Distributed nationwide
  • Sold at government agencies, military distribution +1 more
  • 1,079,883 units affected
Recalled
Added
DeRoyal Industries
Medium RiskFDA Device

DeRoyal Surgical Procedure Packs Recalled for Pencil Malfunction

  • Sold in Ohio
  • Sold at Hospitals, Surgical centers
  • Stryker has received reports that the pencil is activating without manual input; specific injury counts not provided.
Recalled
Added
Merit Medical Systems
Medium RiskFDA Device

Merit Medical Inflation Devices Recalled Due to Handle Detachment Risk

  • Distributed nationwide
  • Sold at authorized medical distributors, hospitals +1 more
  • 4,686,721 units affected
Recalled
Added
Boston Scientific
Critical RiskFDA Device

WATCHMAN Access Systems Recalled by Boston Scientific for Air Embolism Risk

  • Distributed nationwide
  • Sold at Boston Scientific Corporation, Medical distributors +1 more
  • 340,185 units affected
Recalled
Added
Covidien
Medium RiskFDA Device

Chameleon PTA Balloon Catheters Recalled for Potential Pressure Failure

  • Distributed nationwide
  • Sold at Hospital supply chains, Medical device distributors
  • 16,336 units affected
Recalled
Added
Aizu Olympus
Medium RiskFDA Device

Aizu Olympus Co., Ltd.: Various Endoscopes Recalled Due to Risk of Infection from Wet Channels

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Direct Hospital Sales
  • Bacterial Pathogens, Moisture contamination
Recalled
Added
Maquet Cardiovascular
Medium RiskFDA Device

Maquet Cardiovascular, LLC: VasoView HemoPro Systems Recalled for Unintended Cautery and Electrical Failure

  • Distributed nationwide
  • Sold at Hospitals and surgical centers
  • 467,223 units affected
Recalled
Added
Baxter Healthcare
Medium RiskFDA Device

Baxter Healthcare Corporation: Peri-Guard and Supple Peri-Guard Repair Patches Recalled for Neurosurgery Risk

  • Sold in 5 states
  • Sold at Hospitals, Surgical Centers
  • Endotoxins contamination
Recalled
Added
Cardinal Health 200
Medium RiskFDA Device

Cardinal Health 200, LLC: Medical Kits and Trays Recalled Due to Faulty Syringes

  • Distributed nationwide
  • Sold at Cardinal Health, Presource
  • 170,209 units affected
Recalled
Added
Stryker Spine
Medium RiskFDA Device

Stryker Monterey AL Implant Inserters Recalled for Component Separation Risk

  • Sold in 13 states
  • Sold at Stryker Spine, Medical distributors
Recalled
Added
AtriCure
Medium RiskFDA Device

AtriCure, Inc.: Cryo Module Tank Hose Assemblies Recalled for Incorrect Materials

  • Distributed nationwide
  • Sold at Authorized Medical Distributors
Recalled
Added
Critical RiskFDA Device

Olympus Corporation of the Americas: UHI-4 High-Flow Insufflation Units Recalled for Patient Cardiac Arrest Risk

  • Distributed nationwide
  • Sold at Medical distributors, Direct sales to healthcare facilities
  • Reports of patients suffering arrhythmias and short cardiac arrests.
Recalled
Added
Hobbs Medical
Medium RiskFDA Device

Hobbs Medical Posi-Stop Injection Needles Recalled for Blockage and Debris

  • Sold in 15 states
  • Sold at Hospital and medical supply distributors
  • Manufacturing debris contamination
Recalled
Added
Integra LifeSciences
Medium RiskFDA Device

AURORA Surgiscope Systems Recalled for Risk of Obturator Breaking

  • Sold in 20 states
  • Sold at Authorized medical distributors
Recalled
Added
ARROW INTERNATIONAL
Critical RiskFDA Device

ARROW INTERNATIONAL Inc.: Arrow Catheter and PICC Kits Recalled for Incorrect Product Labeling

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