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
Draeger
Critical RiskFDA Device

Draeger Atlan Anesthesia Workstations Recalled for Ventilation Failure

  • Sold in 25 states
  • Sold at Authorized Medical Device Distributors, Direct Hospital Sales
Recalled
Added
Draeger
Critical RiskFDA Device

Draeger Vapor 2000 and 3000 Vaporizers Recalled for Component Impurities

  • Sold in 16 states
  • Sold at Authorized medical device distributors, Direct medical sales
  • Impurities contamination
Recalled
Added
Icotec Ag
Medium RiskFDA Device

Icotec Ag: VADER Pedicle System Torque Wrenches Recalled for Loosening Screws

  • Sold in 10 states
  • Sold at Icotec Ag, Surgical centers/hospitals in AZ, MI, OH, CA, CO, TX, NY, NC, DE, PA
  • One report of a revision surgery required due to loose nut screws.
Recalled
Added
Medium RiskFDA Device

Carefree Surgical Specialties Kittner Roll Gauze Recalled for Contamination

  • Sold in 39 states
  • Sold at Direct distribution
  • biological foreign matter contamination
Recalled
Added
Bard Peripheral Vascular
High RiskFDA Device

Venclose RF Ablation Catheters Recalled for Excessive Temperature Risk

  • Sold in 47 states
  • Sold at Authorized Medical Distributors, Hospitals +1 more
  • 222,373 units affected
Recalled
Added
ROi CPS
Medium RiskFDA Device

ROi CPS LLC: Medical Convenience Kits Recalled for Thin and Non-Uniform Skin Grafts

  • Sold in Missouri
  • Sold at Medical facilities, Hospitals
  • 38 complaints received related to skin grafts being thin and non-uniform
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: Paparrela-Type Vent Tube Recalled for Missing Expiration Date on Packaging

  • Distributed nationwide
  • Sold at Medical distributors, Hospitals
Recalled
Added
Integra LifeSciences
Medium RiskFDA Device

Integra LifeSciences Corp.: Cranial Access Kits Recalled for Potential Sterile Packaging Defects

  • Distributed nationwide
  • Sold at Integra LifeSciences Corp.
Recalled
Added
Ethicon
Medium RiskFDA Device

Ethicon Sutures Recalled for Potential Sterility Breach and Infection Risk

  • Sold in 40 states
  • Sold at Hospital supply channels, Surgical centers
  • Pathogens contamination
Recalled
Added
Medium RiskFDA Device

Hudson RCI mBrace ET Tube Holders Recalled for Skin Injury Risk

  • Distributed nationwide
  • Sold at Hospitals, Medical Supply Distributors
  • Dermal injuries to cheekbones and upper lip noted in complaints.
Recalled
Added
Medium RiskFDA Device

Johnson & Johnson Surgical Vision, Inc.: Irrigation Sleeve Recalled for Missing Port Hole and Eye Surgery Risks

  • Sold in 22 states
  • Sold at Authorized medical distributors
Recalled
Added
Ivenix Infusion System Large Volume Pumps Recalled for Occlusion Alarm Risk
Medium RiskFDA Device

Ivenix Infusion System Large Volume Pumps Recalled for Occlusion Alarm Risk

  • Sold in 21 states
  • Sold at Hospitals, Infusion Centers +1 more
  • 15,862 units affected
Recalled
Added
Medium RiskFDA Device

Medline Nexus Catheter Connectors and Procedure Kits Recalled for Insertion Issues

  • Distributed nationwide
  • Sold at Medline Industries, Hospital supply distributors
  • 21,048 units affected
Recalled
Added
New Medical Technologies
Medium RiskFDA Device

Integra Miltex CryoSolutions Cartridges Recalled for Premature Emptying Risk

  • Sold in 25 states
  • Sold at Authorized medical distributors
Recalled
Added
Ethicon
Medium RiskFDA Device

Ethicon, Inc.: Surgical Sutures Recalled for Compromised Sterility and Infection Risk

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Hospitals +1 more
  • 1,093,500 units affected
Recalled
Added
Trinity Sterile
Medium RiskFDA Device

IMed, Wolf-Pak, and Tacy Medical Dressing Kits Recalled for Packaging Holes

  • Sold in 4 states
  • Sold at IMed Products, Wolf-Pak +1 more
  • 14,140 units affected
Recalled
Added
Tecfen Medical
High RiskFDA Device

Tecfen Medical Ophthalmic Knives Recalled for Potential Lack of Sterility

  • Sold in Connecticut, Minnesota
  • Sold at Medical facilities
Recalled
Added
Boston Scientific
Medium RiskFDA Device

Boston Scientific VersaCross and Torflex Heart Surgery Kits Recalled

  • Distributed nationwide
  • Sold at hospitals, clinical facilities +1 more
  • Microbial Contamination contamination
Recalled
Added
Medium RiskFDA Device

Olympus Resection Sheaths Recalled for Breaking Ceramic Tips

  • Distributed nationwide
  • Sold at Authorized medical distributors, Direct medical sales
  • Complaints received regarding ceramic tips breaking; no specific injury count mentioned.
Recalled
Added
Critical RiskFDA Device

Medline ReNewal Reprocessed Electrophysiology Catheters Recalled for Particulates

  • Distributed nationwide
  • Sold at Hospital and clinical supply channels
  • Residual particulates contamination
Recalled
Added
Medtronic Navigation
Medium RiskFDA Device

Medtronic StealthStation S8 Software Recalled for Spine Surgery Image Errors

  • Sold in 38 states
  • Sold at Medtronic Navigation, Inc., Authorized Medical Distributors
Recalled
Added
Covidien
Medium RiskFDA Device

Covidien, LP: Signia Surgical Stapler Reloads Recalled for Uncontrolled Articulation Risk

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

PALACOS Bone Cement Systems Recalled for Ampoule Breakage Issues

  • Sold at Medical device distributors, Surgical centers
  • Increase of complaints regarding the breakage of the ampoules; no specific injuries were mentioned in the report.
Recalled
Added
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