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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.

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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

StrataMR StrataMR Adjustable Valves And Shunts.

A recall was published by the FDA on 2017-04-07 due to a potential unintended use hazard.


Newport Newport HT70 And Newport HT70 Plus Ventilators

A recall was published by the FDA on 2017-04-05 due to a potential defect hazard.


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.



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