Boston Scientific CRM Corp Recalls

Overview of recall records associated with Boston Scientific CRM Corp, including dates, categories and classifications where available.

2recall records

Oct 29, 2014latest record date

Oct 29, 2014earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceOct 29, 2014

Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the recall — FDA Z-0088-2015

Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs that had experienced an increased rate of premature battery depletion due to compromised performance of a low…

Class IIFDA: TerminatedBoston Scientific CRM Corp

Medical DeviceOct 29, 2014

Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models recall — FDA Z-0087-2015

Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs that had experienced an increased rate of premature battery depletion due to compromised performance of a low…

Class IIFDA: TerminatedBoston Scientific CRM Corp

Understanding this recall history

This page summarizes recall records in which the official source identifies Boston Scientific CRM Corp as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.