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Home > Recalled Products > Medical Devices > Lack of Proper Labeling

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Medical Devices Recalled Due to Lack of Proper Labeling

Since May 01, 2013

Medtronic Trellis-6 And Trellis-8 Peripheral Infusion Systems

A recall was published by the FDA on 2015-02-13 due to a potential lack of proper labeling hazard.


Ultimate Dental and Coltene/Whaledent Non-Latex Dam

A recall was published by the FDA on 2014-09-15 due to a potential lack of proper labeling hazard. Items sold new beginning in .


ADVOCATE Blood Glucose Test Strips

A recall was published by the FDA on 2014-06-10 due to a potential lack of proper labeling hazard.


HeartMate II HeartMate II LVAS Pocket System Controller

A recall was published by the FDA on 2014-03-04 due to a potential lack of proper labeling hazard. Items sold new beginning in May 2013.


Moore/TRUEbalance and Moore/TRUEtrack Blood Glucose Meters

A recall was published by the FDA on 2014-01-07 due to a potential lack of proper labeling hazard. Items sold new beginning in September 2008.



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