Go Backs

Surgical Equipment

AllImplants & Prosthetics(229)Monitoring Devices(257)Diagnostic Equipment(818)Home Healthcare(218)Contact Lenses & Vision(17)Surgical Equipment(896)

896 recalls

per page
Think Surgical
Medium RiskFDA Device

Think Surgical, Inc.: TMINI Array Guide Recalled for Risk of Binding During Drilling

  • Sold in 7 states
  • Sold at Specialized surgical centers, Hospitals
Recalled
Added
FHC
Critical RiskFDA Device

microTargeting Insertion Tube Sets Recalled for Brain Damage Risk

  • Sold in 6 states
  • Sold at Specialty medical distributors
  • 1 complaint received; specific injury details not provided.
Recalled
Added
Boston Scientific
Medium RiskFDA Device

Boston Scientific Coyote Balloon Catheters Recalled for Inflation Issues

  • Sold in 10 states
  • Sold at Medical facilities, Surgical centers +1 more
Recalled
Added
LUMENIS
Medium RiskFDA Device

Lumenis Pulse 120H Laser Systems Recalled for Overheating and Power Failure

  • Sold in Pennsylvania
  • Sold at Authorized medical distributors
Recalled
Added
Biomet
Medium RiskFDA Device

JuggerLoc/ToggleLoc 2.9mm Drill Guides Recalled for Warped Packaging

  • Distributed nationwide
  • Sold at Hospital suppliers, Surgical equipment distributors
Recalled
Added
Stryker
Critical RiskFDA Device

Stryker SmartPump Tourniquet Recalled for Flange Detachment and Leakage Risk

  • Distributed nationwide
  • Sold at Authorized medical distributors, Hospitals +1 more
Recalled
Added
Stryker
Medium RiskFDA Device

Stryker Neptune 3 and S Rovers Recalled for Potential Suction Loss

  • Sold in Washington, Georgia, Illinois
  • Sold at Stryker Corporation
Recalled
Added
Abiomed
Medium RiskFDA Device

Impella 5.5 SmartAssist S2 Recalled for Incorrect Outer Packaging

  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: ESG-410 Electrosurgical Generators Recalled for Power Failures

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas
Recalled
Added
Elekta
Medium RiskFDA Device

Leksell Vantage Stereotactic System Recalled for Paint Flake Risk

  • Sold in 27 states
  • Sold at Hospitals, Surgical Centers +1 more
  • Paint fragments contamination
Recalled
Added
Medium RiskFDA Device

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Allura and Azurion Imaging Systems Recalled for Falling Ceiling Component

  • Distributed nationwide
  • Sold at Philips Medical Systems, Hospital equipment distributors
  • 13,812 units affected
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Perfusion Syringes Recalled for Failed Biocompatibility Testing

  • Sold in California
Recalled
Added
Scientia Vascular
Medium RiskFDA Device

Socrates 38 Aspiration Catheters Recalled for Compromised Sterile Barrier

  • Sold in 18 states
  • Sold at Hospitals, Medical facilities
Recalled
Added
ETHICON
Medium RiskFDA Device

Ethicon STRATAFIX Spiral Knotless Tissue Devices Recalled for Barb Defect

  • Sold in 18 states
  • Sold at Authorized medical distributors, Hospitals +1 more
Recalled
Added
C.R. Bard
High RiskFDA Device

Bardex and Lubri-Sil Foley Catheters Recalled for Potential Blockage Risk

  • Sold in 16 states
  • Sold at Medical Supply Distributors, Hospitals +1 more
  • 175,158 units affected
Recalled
Added
Ethicon
Medium RiskFDA Device

Ethicon, Inc.: SURGIFOAM Absorbable Gelatin Powder Kits Recalled for Open Applicator Seals

  • Sold in 19 states
  • Sold at Authorized medical distributors
Recalled
Added
Covidien
High RiskFDA Device

Covidien, LP: Sofsilk Braided Silk Sutures Recalled for Reduced Strength and Injury Risk

  • Sold at International distributors
Recalled
Added
Orascoptic Surgical Acuity
Medium RiskFDA Device

Orascoptic Surgical Acuity: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.

  • Nickel contamination
  • 26,727 units affected
Recalled
Added
B. Braun Medical
Medium RiskFDA Device

B. Braun Medical, Inc.: Anesthesia Extension Sets Recalled for Potential Product Leakage

  • Distributed nationwide
  • Sold at B. Braun Medical, Inc. distribution channels
  • 19,050 units affected
Recalled
Added
LeMaitre Vascular
Medium RiskFDA Device

LeMaitre Vascular TufTex and Pruitt Catheters Recalled for Package Seal Defect

  • Distributed nationwide
  • Sold at Direct distribution to hospitals, Surgical centers
  • 330,460 units affected
Recalled
Added
Globus Medical
Critical RiskFDA Device

Globus Medical, Inc.: Flat Panel Fluoroscopy Fixture Kit Recalled for Navigation Calibration Error

  • Sold in 5 states
  • Sold at Globus Medical, Inc.
Recalled
Added
Microline Surgical
Medium RiskFDA Device

ReNew Microscissor Tips Recalled for Potential Heat Shrink Detachment

  • Sold in Oklahoma
  • Sold at Specialty medical distributors
Recalled
Added
Medium RiskFDA Device

3M Company - Health Care Business: Durapore Surgical Tape Recalled for Incorrect Shelf Life Labeling

  • Sold in 11 states
  • Sold at Medical supply distributors
  • 3,515,200 units affected
Recalled
Added
Thoratec
High RiskFDA Device

Thoratec CentriMag Blood Pumps Recalled for Motor Locking Failure

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Hospital Supply Chains
  • Particulate contamination
Recalled
Added