Go Backs

Implants & Prosthetics

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

226 recalls

per page
Biomet
Medium RiskFDA Device

Biomet, Inc.: Biolox Ceramic Option Heads Recalled Due to Incorrect Packaging and Sizing

  • Sold in 9 states
  • Sold at Authorized Medical Distributors
  • One product complaint received; no specific injuries reported.
Recalled
Added
Preat
Medium RiskFDA Device

Preat Corp: Neodent GM Healing Abutments Recalled for Potential Microleakage Gap

  • Sold in 7 states
  • Sold at Preat Corp
Recalled
Added
Orthofix U.S.
Medium RiskFDA Device

Virata Polyaxial Screws Recalled for Performance Issues

  • Sold in California, North Carolina, Texas
  • Sold at Authorized Medical Distributors, Hospitals +1 more
Recalled
Added
Nobel Biocare
Medium RiskFDA Device

Nobel Biocare N1 Dental Implants Recalled for Sterility Breach

  • Sold in 11 states
  • Sold at Direct distribution
  • Breach of sterility contamination
Recalled
Added
Tornier
Medium RiskFDA Device

Stryker Latitude EV Humeral Trial Stems Recalled for Incorrect Markings

  • Distributed nationwide
  • Sold at Specialty medical distributors
Recalled
Added
Miach Orthopaedics
Medium RiskFDA Device

BEAR Implant Recalled for Distribution Errors

  • Distributed nationwide
  • Sold at Sales force trunk stock
Recalled
Added
Biomet
Medium RiskFDA Device

Biomet, Inc.: RingLoc Bi-Polar Hip Cup Recalled for Incorrect Locking Ring Assembly

  • Sold in 6 states
  • Sold at hospitals, surgical centers
Recalled
Added
Encore Medical
Medium RiskFDA Device

Encore Medical, LP: EMPOWR Knee Inserts and Hip Liners Recalled for Mislabeled Packaging

  • Sold in 15 states
Recalled
Added
XTANT Medical
Medium RiskFDA Device

XTANT Medical Holdings, Inc: Cortera Spinal Fixation System Screws Recalled for Inadequate Strength Risks

  • Sold in 11 states
  • Sold at Hospitals, Surgical Centers +1 more
Recalled
Added
LeMaitre Vascular
Medium RiskFDA Device

Artegraft Collagen Vascular Graft Recalled for Incorrect Packaging Size

  • Sold in Arkansas
  • Sold at Medical distributors, Hospitals
Recalled
Added
Straumann USA
Medium RiskFDA Device

GM Helix Acqua Implants Recalled for Incorrect Sizing Information

  • Sold in 23 states
  • Sold at Straumann USA LLC
Recalled
Added
Medtronic
Medium RiskFDA Device

Medtronic Inc.: Cobalt XT DR MRI SureScan ICD Recalled for Battery Testing Failure

  • Sold in Florida
  • Sold at Hospitals, Cardiology Clinics
Recalled
Added
Integra LifeSciences
High RiskFDA Device

Integra LifeSciences Corp.: Duraform Dural Graft Implant Recalled for High Endotoxin Levels

  • Sold at Distributors in China
  • Endotoxins contamination
Recalled
Added
Novosource
Medium RiskFDA Device

NovoHip Biolox Ball Head Recalled Due to Mislabeled Packaging

  • Sold in Florida, West Virginia
  • Sold at Specialty medical distributors
Recalled
Added
Alphatec Spine
Medium RiskFDA Device

Alphatec Calibrate CCX Interbody Systems Recalled for Implant Collapse

  • Sold in 24 states
  • Sold at Hospitals, Surgical centers
  • Complaints received regarding post-operative implant collapse; specific injury counts not provided.
Recalled
Added
Medtronic Neuromodulation
Medium RiskFDA Device

Medtronic Neuromodulation: Intellis AdaptiveStim Spinal Cord Stimulator Recalled for Programming Failure

  • Sold at Authorized medical distributors
Recalled
Added
Encore Medical
Medium RiskFDA Device

EMPOWR Dual Mobility Hip Implants Recalled for Packaging Error

  • Sold in 13 states
  • Sold at RFK Medical Inc., Valor Medical Solutions +14 more
Recalled
Added
Exactech
Medium RiskFDA Device

Exactech, Inc.: AcuMatch L-Series Bipolar Hip Liners Recalled for Packaging Defect

  • Sold in Puerto Rico
  • Sold at Authorized Medical Distributors, Hospitals
Recalled
Added
Tornier
Medium RiskFDA Device

Tornier Perform Reversed Peripheral Screws Recalled for Incorrect Labeling

  • Distributed nationwide
  • Sold at Medical distributors, Hospitals
Recalled
Added
Medium RiskFDA Device

LINK MP Reconstruction System Neck Segments Recalled for Labeling Error

  • Sold in Alabama, Florida
  • Sold at Hospitals, Surgical centers
Recalled
Added
Globus Medical
Medium RiskFDA Device

Globus Medical MAGEC 2 Rod System Recalled for Incorrect Diameter

  • Sold in Arkansas
  • Sold at Globus Medical, Inc.
Recalled
Added
Medium RiskFDA Device

MED-EL Elektromedizinische Gereate, Gmbh: Mi1250 SYNCHRONY 2 Cochlear Implants Recalled for Electronics Defect

  • Sold in North Carolina
  • Sold at Specialized medical distributors, Durham NC Distribution Point
Recalled
Added
Preat
Medium RiskFDA Device

Preat Milled Dental Abutments Recalled Due to Manufacturing Defect

  • Sold in 12 states
  • Sold at Dental distributors, Dental practices
Recalled
Added
Preat
Medium RiskFDA Device

Preat Titanium Bases Recalled for Manufacturing Alignment Error

  • Sold in 5 states
  • Sold at Preat Corp
Recalled
Added