Go Backs

Surgical Equipment

AllImplants & Prosthetics(226)Monitoring Devices(267)Diagnostic Equipment(820)Home Healthcare(229)Contact Lenses & Vision(17)Surgical Equipment(891)

891 recalls

per page
Covidien
High RiskFDA Device

Covidien LP: Various Surgical Sutures Recalled for Reduced Strength and Injury Risk

  • Sold in 29 states
  • Sold at Hospital supply distributors, Medical supply retailers
  • 46,812 units affected
Recalled
Added
Getinge Usa Sales
Medium RiskFDA Device

MEERA Mobile Operating Tables Recalled Due to Hand Control Movement Errors

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Getinge Direct Sales
Recalled
Added
Medium RiskFDA Device

MEDLINE INDUSTRIES, LP - Northfield: Medline Surgical Kits Recalled for Incorrectly Labeled Vessel Cannulae

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

Medline Surgical Instruments Recalled for Compromised Sterility Risk

  • Distributed nationwide
  • Sold at Medline Industries, Medical distributors +2 more
  • 21,440 units affected
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon Research LLC: ClearCut and A-OK Ophthalmic Knives Recalled for Reduced Sharpness

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Specialty Ophthalmic Suppliers
  • Increase in complaint reports related to sharpness detected; specific injury counts not provided in the alert text.
Recalled
Added
Maquet Cardiovascular
Medium RiskFDA Device

Maquet Cardiovascular, LLC: Vasoview Hemopro Endoscopic Vessel Harvesting Systems Recalled for Debris Risk

  • Distributed nationwide
  • Sold at hospitals, surgical centers +1 more
  • Polyimide particulate matter contamination
Recalled
Added
Covidien
Medium RiskFDA Device

Covidien, LP: Structural Balloon and Blunt Tip Trocars Recalled for Seal Disengagement

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Hospitals +1 more
  • 774,229 units affected
Recalled
Added
AVID Medical
Medium RiskFDA Device

CLEARIFY Visualization System Recalled for Discoloration from Resterilization

  • Sold in 7 states
  • Sold at Medical facilities, Specialized surgical centers
Recalled
Added
Medium RiskFDA Device

Medline Medical Convenience Kits Recalled for Syringe Quality Issues

  • Distributed nationwide
  • Sold at specialty medical distributors, hospitals +1 more
  • 50,482 units affected
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: Olympus Electrosurgical Generator Recalled for Audio Buffer System Error

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

Beaver Visitec International, Inc.: BVI CustomEyes Procedure Packs Recalled Due to Faulty Syringes

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Hospitals +1 more
  • 38,878 units affected
Recalled
Added
Boston Scientific
Critical RiskFDA Device

Boston Scientific Corporation: Expo 5F Angiographic Catheters Recalled for Potential Lining Detachment

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers +1 more
  • 1,048,538 units affected
Recalled
Added
Medtronic Perfusion Systems
Medium RiskFDA Device

Medtronic Perfusion Systems: Medtronic Perfusion Cannulae and Accessories Recalled for Unsealed Packaging

  • Distributed nationwide
  • Sold at Hospital supply chains, Surgical centers +1 more
  • Potential microbial contamination due to unsealed packaging contamination
Recalled
Added
Carefusion 2200
Medium RiskFDA Device

Carefusion 2200 Inc: Snowden-Pencer Endoscopic Surgical Devices Recalled for Breaking Knobs

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
B. Braun Medical
High RiskFDA Device

B. Braun Medical, Inc.: IV Administration Pump Sets Recalled for Backcheck Valve Malfunction

  • Distributed nationwide
  • Sold at Hospital supply channels, Medical device distributors
  • Reports of patient injuries involving adverse drug reactions and product malfunctions with loss of medication/blood.
Recalled
Added
LSL Healthcare
Medium RiskFDA Device

LSL Healthcare Central Line Dressing Kits Recalled for Packaging Seal Defect

  • Sold in Idaho
  • Sold at Medical distributors
Recalled
Added
Atrium Medical
Medium RiskFDA Device

Atrium Medical Corporation: Ocean, Oasis, and Express Chest Drains Recalled for Missing Instructions

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers +1 more
  • 550,646 units affected
Recalled
Added
Critical RiskFDA Device

MEDLINE INDUSTRIES, LP - Northfield: Medical Kits and Trays Recalled for Possible Lack of Sterility

  • Distributed nationwide
  • Sold at Hospitals, Healthcare facilities +1 more
  • Non-sterile saline, Non-sterile water contamination
Recalled
Added
Alcon Research
Medium RiskFDA Device

Alcon Research LLC: NGENUITY 3D Surgical Image Software Recalled for Incorrect Vision Correction

  • Sold in 34 states
  • Sold at Authorized Medical Distributors, Surgical Centers
Recalled
Added
Medtronic Sofamor Danek USA
Medium RiskFDA Device

Medtronic Sofamor Danek USA Inc: Grafton DBM Bone Matrix Products Recalled for Potential Pouch Non-Conformance

  • Distributed nationwide
  • Sold at Specialty surgical suppliers, Medtronic direct distribution
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Kits with SafeAir Smoke Evacuation Pencils Recalled for Fire Risk

  • Distributed nationwide
  • Sold at medical distributors, surgical center suppliers +1 more
  • 121,300 units affected
Recalled
Added
Medium RiskFDA Device

MEDLINE INDUSTRIES, LP - Northfield: 4.5" Iris Scissors Recalled Due to Potential Sterile Barrier Compromise

  • Distributed nationwide
  • Sold at Hospital supply distributors, Medline Industries
  • 324,451 units affected
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: Olympus Bronchoscopes and Mobilescopes Recalled for Choking and Lodging Risks

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Direct Hospital Sales
  • 41,838 units affected
Recalled
Added
Abbott Vascular
Medium RiskFDA Device

Abbott Cardiovascular Inflation Devices Recalled for Air Embolism Risk

  • Sold in 39 states
  • Sold at Hospitals, Cardiovascular surgery centers
  • 33,473 units affected
Recalled
Added