Go Backs

Implants & Prosthetics

AllImplants & Prosthetics(226)Monitoring Devices(265)Diagnostic Equipment(820)Home Healthcare(225)Contact Lenses & Vision(17)Surgical Equipment(893)

226 recalls

per page
Miach Orthopaedics
Medium RiskFDA Device

BEAR Implant Recalled for Incorrect Expiration Date on Label

  • Sold in 22 states
  • Sold at Hospital and clinical supply chains
Recalled
Added
Zimmer
Medium RiskFDA Device

Zimmer Biomet Ceramic Femoral Heads Recalled for Labeling Defect

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

Encore Medical, LP: Reverse Shoulder Prosthesis Screws Recalled for Incorrect Sizing

  • Sold in 14 states
  • Sold at Hospital supply chains, Medical device distributors
Recalled
Added
Encore Medical
Medium RiskFDA Device

EMPOWR 3D Knee Tibial Inserts Recalled for Packaging Mix-Up

  • Sold in 14 states
  • Sold at Hospitals, Orthopedic surgical centers
Recalled
Added
Centinel Spine
Medium RiskFDA Device

Centinel Spine, Inc.: Prodisc C Total Cervical Discs Recalled for Potential Contamination

  • Distributed nationwide
  • Sold at hospitals, surgical centers
  • foreign contaminate (blue discoloration) contamination
Recalled
Added
IVOCLAR VIVADENT AG
Medium RiskFDA Device

IVOCLAR VIVADENT AG: IPS e.max ZirCAD Dental Blocks Recalled Due to Risk of Cracking and Fracture

  • Distributed nationwide
  • Sold at Ivoclar Vivadent AG, Dental supply distributors
  • 40,138 units affected
Recalled
Added
Orthofix U.S.
Medium RiskFDA Device

Orthofix Pillar SA Ti Spacer System Recalled for Mislabeled Height

  • Sold in California, Colorado, Missouri
  • Sold at Hospitals, Surgical Centers
Recalled
Added
BioPro
Medium RiskFDA Device

BioPro Orthopedic Heads Recalled for Potential Sterile Barrier Breach

  • Sold in Michigan, Texas
  • Sold at Medical device distributors, Hospitals +1 more
Recalled
Added
Zimmer
Medium RiskFDA Device

Zimmer NexGen LCCK Articular Surfaces Recalled for Assembly Defect

  • Sold in 9 states
  • Sold at Hospitals, Surgical Centers
Recalled
Added
GRAPHENANO DENTAL SL
Medium RiskFDA Device

GRAPHENANO DENTAL SL: G-CAM Dental Machining Discs Recalled Due to Machining Errors

  • Sold in Utah
  • Sold at Dental professional distributors
Recalled
Added
Medium RiskFDA Device

NuVasive Precice Max Limb Lengthening Nails Recalled for Design Issues

  • Sold in Florida, Nevada
  • Sold at Hospitals, Surgical centers
Recalled
Added
Encore Medical
Medium RiskFDA Device

Encore Medical Knee and Shoulder Implants Recalled for Incorrect Labeling

  • Sold in 17 states
  • Sold at Hospitals, Surgical Centers
Recalled
Added
Medium RiskFDA Device

Boston Scientific Superion Indirect Decompression Systems Recalled for Breakage

  • Sold in 50 states
  • Sold at Authorized Medical Distributors, Specialized Healthcare Facilities
  • 70,516 units affected
Recalled
Added
Micro Therapeutics
Critical RiskFDA Device

Medtronic Pipeline Vantage Embolization Devices Recalled for Braid Deformation

  • Sold in 48 states
  • Sold at Authorized Medtronic Medical Device Distributors, Specialized Hospitals +1 more
  • Issues noted during procedure and post-procedure at 6-12 month imaging follow-up; potential for thrombosis and serious adverse events.
Recalled
Added
Exactech
Medium RiskFDA Device

Exactech Equinoxe Reverse Shoulder Liners Recalled for Dimensional Specification

  • Sold in 25 states
  • Sold at Hospitals, Surgical Centers +1 more
  • 72,876 units affected
Recalled
Added
Corin
Medium RiskFDA Device

Corin Ltd: Unity CR Knee Inserts Recalled for Incorrect Sizing Labels

  • Sold in Michigan, Texas, Illinois
  • Sold at Medical facilities, Hospitals
Recalled
Added
Smith & Nephew
Medium RiskFDA Device

Smith & Nephew Tandem Bipolar Hip Components Recalled for Oversized Retainer Ring

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers
Recalled
Added
Hiossen
Medium RiskFDA Device

Hiossen and Osstem Dental Abutments Recalled for Mislabeled Chart Stickers

  • Distributed nationwide
  • Sold at Direct distribution from manufacturer
Recalled
Added
CORIN MEDICAL
Medium RiskFDA Device

Apex Knee System Recalled for Potential Loss of Sterile Packaging Integrity

  • Sold in 7 states
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
Inspire Medical Systems
Medium RiskFDA Device

Inspire Medical Systems Inc.: Inspire Respiratory and Stimulation Leads Recalled for Labeling Error

  • Distributed nationwide
  • Sold at Medical facilities, Hospitals +1 more
Recalled
Added
Prismatik Dentalcraft
Medium RiskFDA Device

Inclusive Titanium Screws Recalled for Incorrect Component Packaging

  • Sold in 18 states
  • Sold at Authorized dental distributors
Recalled
Added
Hologic
Critical RiskFDA Device

BioZorb Markers Recalled for Serious Injury and Complication Risks

  • Distributed nationwide
  • Sold at Hologic, Inc., Hospitals +1 more
  • Reports of serious injuries including pain, infection, rash, device migration, device erosion, seroma, and discomfort.
Recalled
Added
XTANT Medical
Medium RiskFDA Device

XTANT Medical Holdings, Inc: Cortera Spinal Fixation Screws Recalled for Incorrect Sizing and Labeling

  • Sold in Michigan
Recalled
Added
Thoratec
Critical RiskFDA Device

Thoratec Corp.: HeartMate 3 LVAS Implant Kits Recalled for Potential Seal Interface Leaks

  • Sold in 41 states
  • Sold at Authorized Medical Distributors, Hospitals
Recalled
Added