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Home Healthcare

AllImplants & Prosthetics(225)Monitoring Devices(272)Diagnostic Equipment(819)Home Healthcare(232)Contact Lenses & Vision(17)Surgical Equipment(890)

232 recalls

per page
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
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
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
Advanced Bionics
Medium RiskFDA Device

HiResolution Bionic Ear M Zn-Air Battery Paks Recalled for Battery Access Risk

  • Sold in 51 states
  • Sold at Authorized Medical Distributors, Audiology Clinics
  • 45,173 units affected
Recalled
Added
WHILL
Critical RiskFDA Device

WHILL, INC.: WHILL Model C2 and Model F Powered Wheelchairs Recalled for Cyber Vulnerability

  • Sold in Kansas
  • Sold at authorized dealers, specialty retailers
Recalled
Added
ZOLIQUEX Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk
High RiskCPSC

ZOLIQUEX Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

  • Distributed nationwide
  • Sold at Amazon.com
  • 16,000 units affected
Recalled
Added
High RiskFDA Device

Uvlizer Germicidal Wand Recalled for Excessive UVC Radiation Risk

  • Distributed nationwide
  • Sold at Uvlizer
  • UVC Radiation contamination
Recalled
Added
Medium RiskFDA Device

Uvlizer Handheld UVC Germicidal Wands Recalled for Excessive Radiation Risk

  • Distributed nationwide
  • Sold at Uvlizer
  • UVC Radiation contamination
Recalled
Added
3B Medical
Medium RiskFDA Device

React Health PHOENIX 5L Oxygen Concentrator Recalled for Quality Defects

  • Sold in New York
  • Sold at Authorized distributors
Recalled
Added
Insulet
Critical RiskFDA Device

Omnipod 5 Pods Recalled for Insulin Leak and Under-Delivery Risk

  • Distributed nationwide
  • Sold at Authorized medical distributors, Pharmacies
  • 1,240,115 units affected
Recalled
Added
High RiskFDA Device

Arjo Tenor Mobile Patient Lifts Recalled for Falling Hazard

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors
Recalled
Added
Beta Bionics
High RiskFDA Device

iLet Ace Pump Kits Recalled for Software Vulnerability and Hypoglycemia Risk

  • Sold in 40 states
  • Sold at authorized distributors
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline and Meijer Sterile Saline Wound Wash Recalled for Sterility Concerns

  • Distributed nationwide
  • Sold at Meijer, Medline Industries +2 more
  • 3,704,376 units affected
Updated
Recalled
EYE COMFORT CARE
Medium RiskFDA Device

EYE COMFORT CARE LLC: UNclog Heated Eye Masks Recalled Due to Short Circuit and Burn Risk

  • Sold in 23 states
Recalled
Added
Ferring Pharmaceuticals
Medium RiskFDA Drug

Ferring Pharmaceuticals Inc: ZOMA-Jet Needle-Free Injector Pens Recalled for Breaking and Disintegrating

  • Distributed nationwide
  • Sold at Pharmacies, Healthcare providers
Recalled
Added
Hospira
Medium RiskFDA Vet

Hospira Inc.: Plum XL Family Infusion Pumps Recalled for Potential Door Roller Failure

  • Sold in 19 states
  • Sold at Hospitals, Home care providers
Recalled
Added
Hospira
Medium RiskFDA Vet

Hospira Inc.: Plum A+ Infusion Pumps Recalled for Potential Alarms and Therapy Interruption

  • Sold in 19 states
  • Sold at Hospira Inc., ICU Medical Inc
Recalled
Added
Hospira
Medium RiskFDA Vet

Hospira Inc.: Plum A+ Infusion System Recalled Due to Potential Fluid Ingress and Pump Failure

  • Sold in 19 states
  • Sold at hospitals, healthcare facilities
Recalled
Added
Aerogen
Medium RiskFDA Vet

Aerogen Ltd.: Aeroneb Nebulizer Power Adapters Recalled for Shock Risk

  • Sold in 6 states
  • Sold at authorized medical distributors
Recalled
Added
Hospira
Medium RiskFDA Vet

Hospira Inc.: Acclaim Encore Infusion Pumps Recalled for Broken Door Assemblies

  • Sold in 47 states
  • Sold at Hospira, Abbott +1 more
Recalled
Added
Caire
High RiskFDA Device

Caire, Inc.: FreeStyle Comfort Oxygen Concentrators Recalled for Battery Charging Failure

  • Distributed nationwide
  • Sold at Authorized medical equipment distributors, Caire, Inc.
Recalled
Added
ConvaTec
Medium RiskFDA Device

Convatec EsteemBody Drainable Pouches Recalled for Potential Leaks

  • Distributed nationwide
  • Sold at Medical supply distributors
Recalled
Added
Navajo Manufacturing
Critical RiskFDA Device

Handy Solutions Heating Pads Recalled for Burn and Fire Risk

  • Sold in 7 states
  • Sold at Retailers in CA, MS, FL, IN, LA, VA, TX
  • 28,457 units affected
Recalled
Added
Medtronic MiniMed
Medium RiskFDA Device

Medtronic MiniMed, Inc.: Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, over-delivery, or cessation of delivery).

  • 26,851 units affected
Recalled
Added