Go Backs

Surgical Equipment

AllImplants & Prosthetics(226)Monitoring Devices(265)Diagnostic Equipment(820)Home Healthcare(226)Contact Lenses & Vision(17)Surgical Equipment(892)

892 recalls

per page
XTANT Medical
Medium RiskFDA Device

XTANT Medical Xpress Pedicle Screw System Recalled for Mislabeled Length

  • Sold in Oregon
  • Sold at hospitals, surgical centers
Recalled
Added
Critical RiskFDA Device

Olympus ViziShot 2 FLEX Aspiration Needles Recalled for Deformed Tips

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas, Medical device distributors
  • 104,508 units affected
Updated
Recalled
Boston Scientific
Medium RiskFDA Device

EndoVive Safety PEG Kits Recalled for Compromised Sterile Packaging

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

Medline Surgical Gowns and Drapes Recalled for Infection Risk

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers +1 more
  • 127,572 units affected
Recalled
Added
Becton Dickinson
Medium RiskFDA Device

BD Luer-Lok Tip Syringes Recalled for Incorrect Syringe Type

  • Sold in California, Texas
  • Sold at Medical distributors, Bulk institutional sales
  • 204,000 units affected
Recalled
Added
Medartis AG
Medium RiskFDA Device

APTUS TriLock Screws Recalled for Sizing Mix-Up

  • Sold in Indiana, Pennsylvania
  • Sold at Medical distributors, Hospitals
Recalled
Added
Exactech
Medium RiskFDA Device

Exactech Equinoxe Ergo Impactor Handles Recalled for Missing Component

  • Sold in 25 states
  • Sold at Direct from manufacturer, Surgical centers +1 more
Recalled
Added
Medline Industries
Medium RiskFDA Device

Cardinal Health Chest Drainage Units Recalled for Incorrect Age Labeling

  • Sold in California
  • Sold at Direct medical distribution, Healthcare facilities
Recalled
Added
International Life Sciences
Medium RiskFDA Device

International Life Sciences Augmentation Devices Recalled for Endotoxin Failure

  • Sold in 41 states
  • Sold at Authorized distributors, Surgical centers +1 more
  • Bacterial endotoxins contamination
Recalled
Added
Stryker
High RiskFDA Device

Stryker Corporation: 1.2mm Cross Cut Fissure Surgical Burrs Recalled for Endotoxin Contamination

  • Distributed nationwide
  • Sold at authorized medical distributors, hospital systems
  • Endotoxins contamination
Recalled
Added
Medium RiskFDA Device

MEDLINE INDUSTRIES, LP - Northfield: 4.5" Sterile Iris Scissors Recalled Due to Loose Tip Protectors

  • Distributed nationwide
  • Sold at Medical supply distributors
  • 67,811 units affected
Recalled
Added
Medium RiskFDA Device

TruDi Navigation System Multi Instrument Adapter Recalled for Inaccuracy

  • Distributed nationwide
  • Sold at Authorized medical device distributors
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: BICOAG Hemostasis Probe Recalled for Labeling and Connector Mismatch

  • Distributed nationwide
  • Sold at international distributors
Recalled
Added
Smiths Medical ASD
Medium RiskFDA Device

Smiths Medical ASD Inc.: Portex Hydrophobic Disc Filters Recalled for Labeling and Expiration Errors

  • Distributed nationwide
  • Sold at Direct medical distribution
  • 66,633 units affected
Recalled
Added
Getinge Usa Sales
Critical RiskFDA Device

Getinge Usa Sales Inc: Sevoflurane Vaporizers Recalled for Potential Hydrogen Fluoride Exposure

  • Sold in 7 states
  • Sold at Getinge Usa Sales Inc
  • Hydrogen fluoride contamination
Recalled
Added
GVS TM
Medium RiskFDA Device

SQ40S Blood Transfusion Filters Recalled for Sterility Concerns

  • Sold in 28 states
  • Sold at Healthcare facilities, Medical distributors
Recalled
Added
Bard Peripheral Vascular
Medium RiskFDA Device

Bard Peripheral Vascular Inc: Mission Core Biopsy Instrument Kits Recalled for Fitting and Access Issues

  • Sold in 52 states
  • Sold at Authorized medical distributors
  • 1,243,937 units affected
Recalled
Added
Integra LifeSciences
Medium RiskFDA Device

Integra LifeSciences Corp.: AURORA Surgiscope System Recalled for Potential Sheath Damage and Bleeding Risk

  • Sold in New York, Ohio, District of Columbia
  • Sold at Integra LifeSciences Corp.
Recalled
Added
Critical RiskFDA Device

Medline Intubation Kits Recalled for Defective Endotracheal Tubes

  • Sold in California
  • Sold at Medical Supply Distributors
Recalled
Added
Barco N.V.
Medium RiskFDA Device

Barco NexxisOR System Components Recalled for Display and Signal Failures

  • Sold in Texas, Ohio
  • Sold at Authorized Medical Device Distributors
Recalled
Added
Maquet Cardiovascular
Medium RiskFDA Device

Maquet Cardiovascular, LLC: Acrobat-i Vacuum Positioners Recalled Due to Arm Locking Failure

  • Distributed nationwide
  • Sold at hospital distributors, Maquet Cardiovascular LLC
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: Quest Spectrum 3 Imaging System Recalled for Electromagnetic Interference Risk

  • Sold in Ohio
  • Sold at Olympus Corporation of the Americas
Recalled
Added
Aesculap Implant Systems
Medium RiskFDA Device

Aesculap Implant Systems LLC: Neuroendoscopy Trocar Recalled for Obstructed Visual Field Risk

  • Sold in 9 states
  • Sold at Direct distribution
Recalled
Added
Medium RiskFDA Device

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Azurion 7 FlexArm Recalled for Software Bug Causing Loss of Movement

  • Sold in 6 states
  • Sold at Authorized Medical Device Distributors, Direct Hospital Sales
Recalled
Added