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
C P Medical
Low RiskFDA Vet

C P Medical: Monofilament Polydioxanone Sutures Recalled for Incorrect Size Labeling

  • Sold in 8 states
  • Sold at Wholesale Medical, Inc., Webster Veterinary Supply +3 more
Recalled
Added
Hospira
Medium RiskFDA Vet

Hospira Inc.: Medical Irrigation and Extension Sets Recalled for Compromised Sterility

  • Sold in 51 states
  • Sold at Hospira Inc., Medical distributors +1 more
  • 2,962,342 units affected
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Sterile Radiology Procedure Kits Recalled for Packaging Breach

  • Sold in Minnesota
  • Sold at authorized distributors
Recalled
Added
Cardinal Health 200
Medium RiskFDA Device

Kendall SCD Comfort Sleeves Recalled for Software Error and Therapy Delay

  • Sold in 5 states
  • Sold at Cardinal Health 200, LLC
Recalled
Added
Tytek Medical
Medium RiskFDA Device

Tytek Medical Inc: Tension Pneumothorax Access Kits Recalled for Instruction and Labeling Updates

  • Sold in Ohio, South Carolina, Virginia
  • 465,572 units affected
Recalled
Added
Insightra Medical
Medium RiskFDA Device

Ultra IABP Catheter Kits Recalled for Unapproved Claims and Use Instructions

  • Sold in 4 states
  • Sold at Hospitals, Medical distributors
  • 24,227 units affected
Recalled
Added
Howmedica Osteonics
Medium RiskFDA Device

MICS3 Angled Sagittal Saw Attachment Recalled for Detachment Risk

  • Distributed nationwide
  • Sold at Hospital and surgical distributors
Recalled
Added
LeMaitre Vascular
Medium RiskFDA Device

Artegraft Vascular Graft Recalled for Packaging and Labeling Mix-Up

  • Sold in Illinois
  • Sold at Medical distributors
Recalled
Added
Erbe USA
Critical RiskFDA Device

Erbe Flexible Cryoprobes Recalled for Rupture and Bursting Risk

  • Distributed nationwide
  • Sold at hospitals, surgical centers +1 more
  • 40,952 units affected
Recalled
Added
Medium RiskFDA Device

Olympus Endoscope Valves and Reprocessors Recalled for Compatibility Defect

  • Distributed nationwide
  • Sold at Authorized Medical Distributors, Direct Sales
  • Biological Contaminants contamination
Recalled
Added
I.T.S.
Medium RiskFDA Device

I.T.S. GmbH Orthopedic Plates and Screws Recalled for MRI Safety Risks

  • Sold in 28 states
  • Sold at Authorized Medical Device Distributors, Surgical Centers +1 more
  • 84,406 units affected
Recalled
Added
Orthalign
Medium RiskFDA Device

Lantern Knee System Drill Plates Recalled for Incorrect Bone Cut Depth

  • Sold in Utah
  • Sold at Hospital systems, Surgical centers
Recalled
Added
Medium RiskFDA Device

Olympus Cutting Forceps Recalled for Jaw Breaking Risk

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas, Surgical equipment distributors
Recalled
Added
Medium RiskFDA Device

Embrace Shoulder Instruments Drill Towers Recalled for Mismatched Article Numbers

  • Sold in 15 states
  • Sold at Authorized surgical distributors
Recalled
Added
Ultradent Products
Medium RiskFDA Device

Jiffy Original Composite Polisher Cups Recalled for Crumbling Risk

  • Sold in 31 states
  • Sold at Dental supply distributors
Recalled
Added
ReCor Medical
Medium RiskFDA Device

Paradise Ultrasound Renal Denervation Catheters Recalled for Scrapped Product

  • Sold in 9 states
  • Sold at Direct distribution to healthcare facilities
Recalled
Added
Stryker Communications
Medium RiskFDA Device

Stryker CHROMOPHARE Softlit Ring Surgical Light System Recalled for Fall Risk

  • Distributed nationwide
  • Sold at Stryker Communications, authorized medical device distributors
Recalled
Added
Medium RiskFDA Device

Olympus SOLTIVE SuperPulsed Laser Systems Recalled for Fire and Smoke Risk

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors
Recalled
Added
Synthes (USA) Products
Medium RiskFDA Device

Synthes Bone Taps Recalled for Incorrect Threading

  • Sold in 21 states
  • Sold at Medical distributors, Hospitals
Recalled
Added
SUMMA THERAPEUTICS
Medium RiskFDA Device

Finesse BTK Multicath Balloon Catheters Recalled for Potential Balloon Burst

  • Sold in New Jersey, Florida
  • Sold at Authorized medical distributors
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

da Vinci S and Si Surgical Instruments Recalled for Broken Grip Cables

  • Sold in 20 states
  • Sold at Authorized Medical Device Distributors, Intuitive Surgical Direct Sales
  • Increased complaints for broken/frayed grip cables (specific counts not provided in description).
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

da Vinci Surgical Instruments Recalled for Frayed or Broken Cables

  • Sold in 24 states
  • Sold at Authorized Medical Distributors, Direct Hospital Sales
  • Increased complaints regarding frayed or broken pitch cables.
Recalled
Added
Civco Medical Instruments
Medium RiskFDA Device

Civco eTRAX Needle Sensors Recalled for Needle Tip Identification Error

  • Sold in Ohio, Pennsylvania, Washington
  • Sold at Medical facilities, Specialty medical distributors
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Medical Kits Recalled for Detachable Biopsy Valve Fragments

  • Sold in 13 states
  • Sold at Authorized Medical Distributors, Hospitals +1 more
  • Rubber fragments contamination
Recalled
Added