feedback
facebook page
Follow Me on Pinterest
twitter page
google plus page
rss feed

Home > Recalled Products > Medical Devices

When reviewing recalls, be sure to check all potentially matching product types. To register belongings for recall information and alerts,
use Items I Own. To check and monitor retail or resale inventory for recalls, use Simply Check.

Narrow Recalls by:


Defect
Contamination
Lack of FDA Approval
Lack of Proper Labeling
Lack of Sterility
Undeclared Ingredients
Particulate Matter
Undetermined Hazard

Medical Device Recalls

Since May 01, 2013

LIFEPAK LIFEPAK 1000 Defibrillator

A recall was published by the FDA on 2017-01-13 due to a potential defect hazard.


Pipeline, Alligator, X-Celerator, more Micro Catheters

A recall was published by the FDA on 2016-10-17 due to a potential defect hazard.


Nurse Assist, Inc. I.V. Flush Syringes

A recall was published by the FDA on 2016-10-04 due to a potential contamination hazard.


Baxter Micron Filters

A recall was published by the FDA on 2016-10-03 due to a potential particulate matter hazard.


Roadrunner UniGlide Hydrophilic Wire Guides

A recall was published by the FDA on 2016-08-15 due to a potential contamination hazard.


Alere INRatio, Alere INRatio2 Monitoring System

A recall was published by the FDA on 2016-07-12 due to a potential unintended use hazard.


Beacon, Shuttle, Fluoro-Set, and others Catheters With Beacon Tip Technology

A recall was published by the FDA on 2016-05-03 due to a potential defect hazard.


Covidien Oridion Capnostream 20 And 20p Patient Monitors

A recall was published by the FDA on 2016-04-20 due to a potential defect hazard.



<< Prev | 1 | 2 | 3 | Next >>