Boston Scientific CRM Corp: Boston Scientific LIVIAN Cardiac Resynchronization Therapy Defibrillator (CRT-D), models H220, H225, H227, H229. The LIVIAN family of cardiac resynchronization therapy defibrillators (CRT-Ds), provide ventricular tachyarrhythmia and cardiac resynchronization therapies. Ventricular tachyarrhythmia therapy is for the treatment of ventricular tachycardia (VT) and ventricular fibrillation (VF), rhythms that are associated with sudden cardiac death (SCD). Cardiac resynchronization therapy is for the treatment of heart failure(HF) and uses biventricular electrical stimulation to synchronize ventricular contractions. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue, St. Paul, MN 55112-5798 USA.

Recall number

Z-1556-2010

Recalling firm

Boston Scientific CRM Corp

Product

Boston Scientific LIVIAN Cardiac Resynchronization Therapy Defibrillator (CRT-D), models H220, H225, H227, H229. The LIVIAN family of cardiac resynchronization therapy defibrillators (CRT-Ds), provide ventricular tachyarrhythmia and cardiac resynchronization therapies. Ventricular tachyarrhythmia therapy is for the treatment of ventricular tachycardia (VT) and ventricular fibrillation (VF), rhythms that are associated with sudden cardiac death (SCD). Cardiac resynchronization therapy is for the treatment of heart failure(HF) and uses biventricular electrical stimulation to synchronize ventricular contractions. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue, St. Paul, MN 55112-5798 USA.

Status

Terminated

Initiated

2010-03-15

Posted

2010-05-08

Terminated

2012-04-05

Reason

Boston Scientific Corporation has stopped shipment and is retrieving unimplanted devices from US hospital shelves of all its implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) after determining that some manufacturing process changes were not submitted for approval to the US Food & Drug Administration.

Root cause

PMA

Action

BSC issues press release dated 15 March 2010. FDA press release posted 18 March 2010. On 15 March 2010, BSC Sales Representatives begin removal of devices from health care facilities stock. Starting 22 March 2010 BSC sent a physician letter dated 22 March 2010 to implanting and following physicians via FedEx. The Urgent Medical Device Recall letter described the issue of why devices were being removed from hospital shelves. The letter did NOT recommend any changes to normal follow-up procedures for patients implanted with an ICD or CRT-D device. The letter included ALL potential US models. To be complete and mitigate the possibility of retrieval errors, the ICD and CRT-D US models that may be on customer's shelves were included in the letter. The devices subject to retrieval, however, were those non-implanted devices with domestic customers. For questions, please contact the local representative (1-800-227-3422) for pick up and return or contact Boston Scientific Technical Services at 1.800.CARDIAC (227.3422).

Quantity

135

Distribution

nationwide within US only (OUS distribution not affected).

Lot, serial or model codes

Model H220, serial numbers: 511302, 512322, 513553, 513555, 513592, 513617, 513637, 513638, 513641, 513653, 513741, 513876, 513883, 513886, 513888, 513906, 513940, 513951, 513954, 513988, 514010, 514029, 514033, 514041, 514044, 514047, 514060, 514065, 514070, 514080, 514105, 514107, 514121, 514129.  Model H225, serial numbers: 562014, 562031, 562033, 562040, 562067, 562080, 562116, 562124, 562129, 562133.  Model H227, serial numbers: 511024, 561060, 561618, 562179, 562439, 562789, 563298, 563319, 563323, 563342, 563350, 563366, 563391, 563395, 563400, 563411, 563470, 563484, 563532, 563535, 563547, 563589, 563608, 563615, 563616, 563624, 563662, 563714, 563771, 563785, 563799, 563801, 563804, 563820, 563823, 563824, 563825, 563829, 563831, 563832, 563833, 563840, 563845, 563846, 563847, 563852, 563853, 563854, 563855, 563908, 563918, 563934, 563957, 563962, 563967, 563970, 563972, 563976.  Model H229, serial numbers: 560803, 560813, 560837, 560872, 560873, 560891, 560918, 560921, 560946, 560958, 560959, 560968, 560978, 560985, 561002, 561006, 561021, 561023, 561028, 561030, 561036, 561040, 561057, 561061, 561069, 561073, 561077, 561080, 561092, 561095, 561155, 561158, 561160.

510(k) numbers

not on file

PMA numbers

["P010012"]

Product code

LWP

Firm FEI

2124215

Firm city

Saint Paul

Firm state

MN

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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