Boston Scientific CRM Corp: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: March 27, 2013. Most recent: October 29, 2014.

Risk classification: Class II: 8

Most recent recalls

DateAgencyProduct
October 29, 2014FDABoston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the follo…Z-0088-2015
October 29, 2014FDABoston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N…Z-0087-2015
August 13, 2014FDABoston Scientific ENDOTAK RELIANCE¿ SG, transvenous defibrillation lead, Models 0180 & 02…Z-2147-2014
October 23, 2013FDABoston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the follo…Z-0026-2014
October 23, 2013FDABoston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N…Z-0025-2014
August 28, 2013FDABoston Scientific, ENERGEN DR ICD, Model E143. The device is an Implantable Cardioverter …Z-1979-2013
May 29, 2013FDALATITUDE¿ Patient Management System, Model 6488, Version 7.3. The LATITUDE Patient Man…Z-1339-2013
March 27, 2013FDABoston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse generators. The S-IC…Z-0965-2013

Questions about this company

How many recalls does Boston Scientific CRM Corp have?
Recalert has 8 U.S. recalls on record for Boston Scientific CRM Corp, published between March 27, 2013 and October 29, 2014.
What was the most recent Boston Scientific CRM Corp recall?
FDA recall Z-0088-2015, published October 29, 2014: Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models E103, E111, F102, F103, F110, F111. Sterilized using ethylene…
Which agencies have handled Boston Scientific CRM Corp recalls?
Boston Scientific CRM Corp appears as the recalling firm in recalls from: FDA (8).

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