Go Backs

Home Healthcare

AllImplants & Prosthetics(226)Monitoring Devices(263)Diagnostic Equipment(818)Home Healthcare(223)Contact Lenses & Vision(17)Surgical Equipment(895)

223 recalls

per page
Max Mobility
Critical RiskFDA Device

Max Mobility Permobil SmartDrive SpeedControl Dials Recalled for Loss of Control

  • Sold in 52 states
  • Sold at Permobil, authorized medical equipment dealers
  • Potential for minor and major injuries due to loss of control.
Recalled
Added
Kinova
Critical RiskFDA Device

Kinova Inc: Jaco Assistive Robot Arms Recalled for Potential Fire Hazard

  • Sold in 4 states
  • Sold at Authorized medical device distributors
Recalled
Added
ResMed
Critical RiskFDA Device

ResMed Ltd.: ResMed Non-Invasive Masks Recalled for Potential Magnetic Interference

  • Distributed nationwide
  • Sold at Authorized ResMed dealers, Medical supply companies
  • 28,748,349 units affected
Recalled
Added
Thor Photomedicine
Medium RiskFDA Device

Thor Photomedicine Ltd: Whole Body Red Light Therapy Beds Recalled for Detaching Canopy Struts

  • Sold in 22 states
  • Sold at Authorized distributors, Medical specialty providers
Recalled
Added
Baxter Healthcare
Medium RiskFDA Device

Baxter Healthcare Corporation: Amia Automated Peritoneal Dialysis Cycler Sets Recalled for Failure Alarms

  • Distributed nationwide
  • Sold at Baxter Healthcare Corporation, Medical distributors
  • 339,936 units affected
Recalled
Added
Busse Hospital Disposables, Inc.: Tracheostomy and Dressing Kits Recalled for Risk of Non-Sterile Saline
Critical RiskFDA Device

Busse Hospital Disposables, Inc.: Tracheostomy and Dressing Kits Recalled for Risk of Non-Sterile Saline

  • Distributed nationwide
  • Sold at Hospitals, Medical Supply Distributors
Recalled
Added
GOLD STAR DISTRIBUTION
Medium RiskFDA Device

Trojan, Always, and Oral B Personal Care Products Recalled for Rodent Activity

  • Sold in Minnesota
  • Sold at Authorized retailers in Minnesota
  • Rodents, Rodent activity contamination
Recalled
Added
Baxter Healthcare
Critical RiskFDA Device

Welch Allyn Life2000 Ventilators Recalled for Failure to Alarm

  • Distributed nationwide
  • Sold at Authorized medical distributors, Healthcare facilities
  • 10,957 units affected
Recalled
Added
Medium RiskFDA Device

ARJOHUNTLEIGH POLSKA Sp. z.o.o.: Arjo Medical Beds with IndiGo Drive Modules Recalled for Unintended Movement

  • Sold in 7 states
  • Sold at Authorized Arjo distributors, Medical equipment providers
Recalled
Added
ConvaTec
Medium RiskFDA Device

ConvaTec, Inc: EsteemBody Soft Convex Drainable Pouches Recalled for Filter Weld Defects

  • Distributed nationwide
Recalled
Added
Avanos Medical
Low RiskFDA Device

Avanos Medical, Inc.: NEOMED Pharmacy Syringes Recalled Due to Missing Expiration Dates

  • Distributed nationwide
  • Sold at Avanos Medical, Inc., Pharmacy distributors +1 more
  • 79,242 units affected
Recalled
Added
Baxter Healthcare
Medium RiskFDA Device

Baxter Healthcare Corporation: SIGMA Spectrum Infusion Pump Recalled for Improper Testing Prior to Release

  • Sold in Florida
  • Sold at Direct distribution
Recalled
Added
Outset Medical
Medium RiskFDA Device

Outset Medical, Inc.: Tablo Hemodialysis Console Recalled for Faulty Blood Leak Sensor

  • Sold in 46 states
  • Sold at Authorized Medical Device Distributors, Hospitals +1 more
Recalled
Added
Philips Respironics
Medium RiskFDA Device

SimplyGo Mini Battery Kits Recalled for Potential Oxygen Supply Failure

  • Sold in 5 states
  • Sold at Authorized medical equipment dealers, Direct distribution
Recalled
Added
RECORDATI RARE DISEASES
Medium RiskFDA Device

Caphosol Artificial Saliva Recalled for Stability Test Failure

  • Sold in 5 states
Recalled
Added
Advanced Bionics
Medium RiskFDA Device

HiResolution Bionic Ear System M Battery Chargers Recalled for Mislabeling

  • Sold in 6 states
  • Sold at Advanced Bionics authorized distributors
Recalled
Added
Philips Respironics
Critical RiskFDA Device

DreamStation CPAP and BiPAP Machines Recalled for Programming Error

  • Sold in 14 states
  • Sold at Medical equipment suppliers, Authorized dealers
Recalled
Added
Unomedical A/S
Medium RiskFDA Device

Unomedical A/S: VariSoft Infusion Sets Recalled for Packaging Error and Incorrect Brand Labeling

  • Sold in California
  • Sold at Osted
Recalled
Added
OptumHealth Care Solutions
Critical RiskFDA Device

OptumHealth Care Solutions LLC: Nimbus II Plus Infusion Pumps Recalled for Potential Failure and Leakage

  • Distributed nationwide
  • Sold at OptumHealth Care Solutions LLC
Recalled
Added
ConvaTec
Medium RiskFDA Device

ConvaTec, Inc: ConvaTec CarboFlex Odor Control Dressings Recalled for Sterility Issues

  • Sold in 6 states
Recalled
Added
ResMed
Critical RiskFDA Device

ResMed Ltd.: Astral 100 and Astral 150 Ventilators Recalled for Sudden Power Loss

  • Sold in 47 states
  • Sold at medical equipment suppliers, healthcare providers
  • 55,279 units affected
Recalled
Added
SoClean
Medium RiskFDA Device

SoClean, Inc: SoClean 2 and 3 Maintenance Systems Recalled Due to Ozone Gas Exposure Risk

  • Distributed nationwide
  • Sold at authorized dealers, specialty retailers
  • Ozone gas contamination
Recalled
Added
Baxter Healthcare
Medium RiskFDA Device

Baxter Healthcare Corporation: Hill-Rom PRO+ Mattress Surfaces Re-evaluated for Service Record Errors

  • Sold in Colorado
  • Sold at Authorized Medical Distributors
Recalled
Added
3B Medical
Medium RiskFDA Device

3B Medical Ultrasoft Oxygen Cannulas Recalled for Use Past Expiration Date

  • Sold in Massachusetts, Arkansas
  • Sold at medical equipment distributors
Recalled
Added