Go Backs

Medical Devices

Medical Devices product recalls

AllImplants & Prosthetics(224)Monitoring Devices(272)Diagnostic Equipment(820)Home Healthcare(233)Contact Lenses & Vision(17)Surgical Equipment(890)

2,693 recalls

per page
Spacelabs Healthcare
Medium RiskFDA Device

Spacelabs SL Command Module Recalled for Electrical Safety Issue

  • Sold in 7 states
  • Sold at Direct distribution to hospitals/clinics
Recalled
Added
Centinel Spine
Medium RiskFDA Device

Centinel Spine Prodisc C SK Cervical Discs Recalled for Labeling Mix-Up

  • Sold in 8 states
  • Sold at Authorized medical distributors, Direct to hospitals
Recalled
Added
AVID Medical
Critical RiskFDA Device

Halyard and Cardiac Cath Kits Recalled for Syringe Disconnection Risk

  • Sold in 7 states
  • Sold at Hospitals, Surgical Centers +1 more
  • 19,413 units affected
Recalled
Added
Cook
Critical RiskFDA Device

Cook Sizing Catheters Recalled for Marker Band Cracking and Breakage

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Hospitals
  • 15,769 units affected
Recalled
Added
Boston Scientific
Medium RiskFDA Device

Boston Scientific LUX-Dx ICM Devices Recalled for Monitoring Failure

  • Distributed nationwide
  • Sold at Direct from manufacturer, Hospitals +1 more
Recalled
Added
Erbe Medical
Medium RiskFDA Device

Erbe Medical ERBEFLO CleverCap and Tubing Recalled for Aspiration Risk

  • Sold in 52 states
  • Sold at Authorized Medical Distributors, Direct Sales to Hospitals/Clinics
  • 289,821 units affected
Recalled
Added
Intuitive Surgical
Medium RiskFDA Device

da Vinci X and Xi Surgical Systems Recalled for Breaking Arm Screws

  • Sold in 49 states
  • Sold at Direct Sales, Hospital Distributors
Recalled
Added
Ventec Life Systems
Critical RiskFDA Device

Ventec VOCSN V+Pro Ventilators Recalled for Oxygen Leak and Fire Risk

  • Sold in 4 states
  • Sold at Medical equipment distributors
Recalled
Added
Intuitive Surgical
Critical RiskFDA Device

Intuitive 8 mm SureForm 30 Gray Reloads Recalled for Incomplete Staple Line

  • Sold in 49 states
  • Sold at Hospitals, Surgical Centers
Recalled
Added
Hepo Adult Portable Bed Rails Recalled for Entrapment and Suffocation Risks
Critical RiskCPSC

Hepo Adult Portable Bed Rails Recalled for Entrapment and Suffocation Risks

  • Distributed nationwide
  • Sold at Walmart.com, Amazon.com
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline and Centurion Medical Kits Recalled for Non-Sterile Alcohol Pads

  • Distributed nationwide
  • Sold at Hospital supply distributors, Medical supply channels
  • Paenibacillus phoenicis contamination
Recalled
Added
DEPUY (IRELAND)
Medium RiskFDA Device

Depuy Synthes Attune Revision Hinge Femoral Implants Recalled

  • Sold in Minnesota, North Carolina, Texas
  • Sold at Hospital and clinical supply chains
Recalled
Added
Immuno-Mycologics
Medium RiskFDA Device

Immy Neutralization Buffer B Recalled for Potential Contamination

  • Sold in 11 states
  • Sold at Clinical laboratories, Medical distributors
  • Unknown contaminants contamination
Recalled
Added
North American Rescue
Critical RiskFDA Device

North American Rescue AIDBAGs Recalled for Faulty Glucose Meter Software

  • Sold in California, Washington
  • Sold at specialty first aid kit providers
Recalled
Added
Straumann USA
Medium RiskFDA Device

Straumann n!ce Dental Implant Restorations Recalled for Incorrect Screw Seat

  • Sold in 8 states
  • Sold at Dental clinics, Oral surgery centers +1 more
Recalled
Added
Medium RiskFDA Device

Siemens epoc BGEM BUN Test Cards Recalled for Inaccurate Results

  • Distributed nationwide
  • Sold at Authorized distributors
  • 71,725 units affected
Recalled
Added
Becton Dickinson
Medium RiskFDA Device

BD GasPak EZ CO2 and Campy Pouch Systems Recalled for Low Gas Levels

  • Distributed nationwide
  • Sold at Wholesalers, Direct distribution
  • 27,960 units affected
Recalled
Added
Merit Medical Systems
Medium RiskFDA Device

Philips Bridge Prep Kit Recalled for Catheter Advancement Issues

  • Sold in Colorado
  • Sold at Medical distributors
Recalled
Added
Abbott Point Of Care
High RiskFDA Device

i-STAT Cartridges Recalled for Potential False Blood Gas Results

  • Distributed nationwide
  • Sold at Authorized medical distributors
  • 440,700 units affected
Recalled
Added
Elekta
Medium RiskFDA Device

Leksell Vantage Arc System Recalled for Potential Coordinate Shifting

  • Sold in 32 states
  • Sold at Elekta, Inc. Authorized Distributors
Recalled
Added
Low RiskFDA Device

Heraeus Medical PALAMIX Mixing Devices Recalled for Reduced Shelf Life

  • Distributed nationwide
  • Sold at dental supply distributors, specialty dental retailers
  • 52,896 units affected
Recalled
Added
Beta Bionics
High RiskFDA Device

iLet Bionic Pancreas Recalled for Software-Related Dosing Issues

  • Sold in 8 states
  • Sold at authorized medical device distributors
Recalled
Added
Biomerieux
Medium RiskFDA Device

VITEK 2 Gram-negative Susceptibility Cards Recalled for Testing Failures

  • Distributed nationwide
  • Sold at Direct distribution to laboratories and hospitals
  • 2,668,954 units affected
Updated
Recalled
Medium RiskFDA Device

Dimension Creatinine Flex Reagent Cartridges Recalled for Inaccurate Results

  • Distributed nationwide
  • Sold at Siemens Healthcare Diagnostics, Laboratory supply distributors
  • 18,080 units affected
Recalled
Added