Recall · FDA

Boston Scientific Corporation

Boston Scientific Corporation issued a Class II FDA recall (Z-3256-2018) initiated 2018-09-10: PROPONENT Pacemaker

CompanyBoston Scientific Corporation
Recall numberZ-3256-2018
ClassificationClass II
StatusTerminated
CategoryDevices
Initiated2018-09-10
ProductPROPONENT Pacemaker
ReasonBoston Scientific has identified a subset of active pacemaker and CRT-Ps systems with an elevated potential for early pacemaker replacement due to hydrogen-induced accelerated battery depletion.

FAQ

What did Boston Scientific Corporation recall?

PROPONENT Pacemaker

Why was Boston Scientific Corporation's product recalled?

Boston Scientific has identified a subset of active pacemaker and CRT-Ps systems with an elevated potential for early pacemaker replacement due to hydrogen-induced accelerated battery depletion.

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