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
S.I.N. Implant System Ltda
Medium RiskFDA Device

S.I.N. Implant System Dental Implants Recalled for Improper Storage Conditions

  • Sold in 37 states
  • Sold at Authorized dental device distributors, Medical specialty suppliers
Recalled
Added
Onkos Surgical
Medium RiskFDA Device

My3D Personalized Solutions Humeral Cup Recalled for Missed Quality Inspections

  • Sold in Maryland
  • Sold at Surgical centers, Hospitals
Recalled
Added
Smith & Nephew
Medium RiskFDA Device

Smith & Nephew Inc: LEGION Knee Implant Recalled for Packaging and Labeling Error

  • Sold in 7 states
  • Sold at hospitals, surgical centers
Recalled
Added
Integra LifeSciences
Medium RiskFDA Device

Codman CERTAS Plus Programmable Valves Recalled for Incorrect Labeling

  • Sold in 22 states
  • Sold at Hospitals, Surgical centers +1 more
Recalled
Added
Medtronic Neuromodulation
Medium RiskFDA Device

Medtronic Neuromodulation: Percept RC Implantable Neurostimulators Recalled for Communication Failure

  • Distributed nationwide
  • Sold at Medtronic Neuromodulation, authorized medical distributors
Recalled
Added
United Orthopedic
Medium RiskFDA Device

United Orthopedic Corporation: USTAR II Hip and Knee Systems Recalled for Potential Incorrect Stem Orientation

  • Sold in 9 states
  • Sold at Orthopedic surgeons, Hospitals +1 more
Recalled
Added
TMJ Solutions
Medium RiskFDA Device

TMJ Solutions Inc: TMJ Unilateral Implant Recalled for Incorrect Components

  • Sold in Minnesota
  • Sold at TMJ Solutions Inc
Recalled
Added
Moximed
Medium RiskFDA Device

Moximed MISHA Knee System Implants Recalled for Potential Component Fracture

  • Sold in 7 states
  • Sold at Hospitals, Orthopedic surgical centers
Recalled
Added
CORNEAT VISION
Medium RiskFDA Device

CorNeat EverPatch Recalled for Labeling Correction on Wound Dehiscence

  • Sold in 28 states
  • Sold at Authorized medical distributors
  • Complaints received (specific injury counts not provided)
Recalled
Added
Paragon 28
Medium RiskFDA Device

Paragon 28, Inc.: Phantom TTC Nails Recalled for Distribution Prior to Sterilization

  • Sold in California
  • Sold at Healthcare facilities, Hospitals
Recalled
Added
Stryker
Medium RiskFDA Device

Stryker GAMMA4 Right Long Nail Recalled for Incorrect Left-Side Geometry

  • Sold in 4 states
  • Sold at Hospital networks, Surgical centers +1 more
Recalled
Added
Straumann USA
Low RiskFDA Device

Straumann WB Impression Posts Recalled for Incorrect Impression Caps

  • Distributed nationwide
  • Sold at authorized dental distributors, direct sales
Recalled
Added
Tornier
Medium RiskFDA Device

Tornier, Inc: Perform Reversed Inserts Recalled for Improperly Assembled Locking Ring

  • Distributed nationwide
  • Sold at Hospitals, Surgical Centers
Recalled
Added
Smith & Nephew
Medium RiskFDA Device

Smith & Nephew Inc: OXINIUM Femoral Heads Recalled for Incorrect Size Labeling

  • Distributed nationwide
  • Sold at Specialty medical distributors, Hospitals
Recalled
Added
Smith & Nephew
Medium RiskFDA Device

Smith & Nephew Knee Implants Recalled for Mismatched Components

  • Sold in 7 states
  • Sold at Authorized medical distributors
Recalled
Added
Smith & Nephew
Medium RiskFDA Device

Smith & Nephew LEGION OXINIUM Knee Implants Recalled for Incorrect Labeling

  • Sold in Texas
  • Sold at hospitals, surgical centers +1 more
Recalled
Added
Meddev
Medium RiskFDA Device

Contour Gold Eyelid Weight Implants Recalled for Mislabeling

  • Sold in 17 states
  • Sold at Direct medical distribution
Recalled
Added
Encore Medical
Medium RiskFDA Device

Encore Medical, LP: EMPOWR Porous Knee Systems Recalled for Incorrect Device Packaging

  • Distributed nationwide
  • Sold at Authorized medical distributors, Direct hospital sales
Recalled
Added
Limacorporate S.p.A
Medium RiskFDA Device

Limacorporate TEMA Elbow Prosthesis Recalled for Tool Incompatibility

  • Sold in Florida, Texas
  • Sold at Specialty medical distributors, Hospitals
Recalled
Added
Treace Medical Concepts
Medium RiskFDA Device

Treace Medical Concepts, Inc.: Nanoplasty 3D Bunion Correction System Recalled for Potential Screw Stripping

  • Sold in 8 states
  • Sold at Specialized medical distributors, Direct to hospitals/surgical centers
Recalled
Added
Preat
Medium RiskFDA Device

Preat Corp: Astra EV 4.8mm Milled Titanium Abutments Recalled for Mislabeled Packaging

  • Sold in California, Missouri, Nevada
  • Sold at Dental clinics, Surgical centers
Recalled
Added
Medium RiskFDA Device

Tribio Implant Recalled for Incorrect Product Name Labeling

  • Sold in Tennessee
  • Sold at Medical distributors and healthcare facilities
Recalled
Added
Angel Medical Systems
High RiskFDA Device

The Guardian Cardiac Diagnostic Implant Recalled for Premature Battery Failure

  • Sold in 11 states
  • Sold at Specialized medical providers
Recalled
Added
SCIENCE & BIO MATERIALS
Medium RiskFDA Device

Bio 1 Implant Bone Granules Recalled for Underfilled Vials

  • Distributed nationwide
  • Sold at Authorized medical distributors
Recalled
Added