Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Boston ScientificLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Boston Scientific CRM Corp with 8 device recalls. The most recent is a device recall dated Sep 17, 2014: Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the foll….
| Sep 17, 2014 | Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models E10Class II · Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs that had experienced an increased rate of pr | Device recalls |
| Sep 17, 2014 | Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following models are not available iClass II · Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs that had experienced an increased rate of pr | Device recalls |
| Jun 19, 2014 | Boston Scientific ENDOTAK RELIANCE¿ SG, transvenous defibrillation lead, Models 0180 & 0292, Sterile EO. Product Usage: The ENDOTAK RELIClass II · A review of manufacturing test records for Boston Scientific ENDOTAK RELIANCE implantable leads revealed a suspected te | Device recalls |
| Aug 29, 2013 | Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models F10Class II · The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and TELIGEN ICDs manufactured prior to December | Device recalls |
| Aug 29, 2013 | Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following models are not available iClass II · The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and TELIGEN ICDs manufactured prior to December | Device recalls |
| Jul 15, 2013 | Boston Scientific, ENERGEN DR ICD, Model E143. The device is an Implantable Cardioverter Defibrillator.Class II · Boston Scientific CRM manufacturing quality system recently discovered test artifacts (related to shock charge time) in | Device recalls |
| Apr 10, 2013 | LATITUDE¿ Patient Management System, Model 6488, Version 7.3. The LATITUDE Patient Management system is intended for use to remotely commClass II · Boston Scientific CRM is conducting a recall on the LATITUDE Patient Management System Model 6488 Version 7.3 because | Device recalls |
| Mar 1, 2013 | Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse generators. The S-ICD System is intended to provide therapy for the treClass II · An internal protective fuse can be unintentionally activated while the device is charging its capacitors for shock deliv | Device recalls |
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