Almost exactly a year after beginning a recall of some of its implantable defibrillator devices that were found to potentially emit electrical pulses below their programmed strength, Medtronic has ...
Please provide your email address to receive an email when new articles are posted on . Medtronic recalled ICDs and CRT-Ds with a glassed feedthrough made after Oct. 13, 2017 due to risk for low- or ...
MINNEAPOLIS -- Medtronic has issued a recall for over 348,000 defibrillators because there is a risk they deliver low shock, or no shock at all. The Class I recall - the most serious type of recall ...
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