FDA Device recall Z-0026-2014

Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models F1…

FDA Device
Class II
terminated
Published 2013-10-23

On 2013-10-23 the FDA classified a Class II recall of Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models F1… by Boston Scientific Crm, citing the performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and TELIGEN ICDs manufactured prior to December 2009, may be compromised over time, causing increased curre….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0026-2014
Classification	Class II
Status	terminated
Initiated	2013-08-29
Published	2013-10-23
Last updated	2026-09-13 11:53 UTC
Company	Boston Scientific Crm
Distribution	US

Product

Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models F102, F110, F111. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Indicated for patients who are at risk for sudden cardiac death due to ventricular arrhythmias and may require pacing support.

Reason

The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and TELIGEN ICDs manufactured prior to December 2009, may be compromised over time, causing increased current drain that can lead to premature battery depletion.

Identifiers

code_info	Model E102, Serial Numbers: 000138, 000139, 000140, 000142, 000145, 000146, 000147, 000151, 000152, 000153, 000154, 00… Model E102, Serial Numbers: 000138, 000139, 000140, 000142, 000145, 000146, 000147, 000151, 000152, 000153, 000154, 000161, 000162, 000163, 000166, 000167, 000169, 000170, 000172, 000173, 000174, 000175, 000176, 000177, 000178, 000182, 000183, 000184, 000185, 000187, 000188, 000191, 000192, 000193, 000194, 000196, 000199, 000200, 000202, 000203, 000204, 000207, 000209, 000210, 000213, 000214, 000215, 000216, 000218, 000219, 000220, 000221, 000222, 000224, 000226, 000227, 000228, 000229, 000230, 000232, 000234, 000235, 000236, 000240, 000241, 000244, 000247, 000248, 000249, 000251, 000252, 000254, 000256, 000258, 000260, 000262, 000263, 000265, 000266, 000268, 000269, 000270, 000271, 000272, 000273, 000274, 000275, 000276, 000277, 000278, 000282, 000284, 000287, 000288, 000289, 000290, 000292, 000294, 000295, 000297, 000299, 000300, 000302, 000304, 000306, 000307, 000309, 000310, 000311, 000314, 000316, 000321, 000322, 000323, 000324, 000325, 000330, 000332, 000334, 000335, 000337, 000

code_info

Model E102, Serial Numbers: 000138, 000139, 000140, 000142, 000145, 000146, 000147, 000151, 000152, 000153, 000154, 00…

Model E102, Serial Numbers: 000138, 000139, 000140, 000142, 000145, 000146, 000147, 000151, 000152, 000153, 000154, 000161, 000162, 000163, 000166, 000167, 000169, 000170, 000172, 000173, 000174, 000175, 000176, 000177, 000178, 000182, 000183, 000184, 000185, 000187, 000188, 000191, 000192, 000193, 000194, 000196, 000199, 000200, 000202, 000203, 000204, 000207, 000209, 000210, 000213, 000214, 000215, 000216, 000218, 000219, 000220, 000221, 000222, 000224, 000226, 000227, 000228, 000229, 000230, 000232, 000234, 000235, 000236, 000240, 000241, 000244, 000247, 000248, 000249, 000251, 000252, 000254, 000256, 000258, 000260, 000262, 000263, 000265, 000266, 000268, 000269, 000270, 000271, 000272, 000273, 000274, 000275, 000276, 000277, 000278, 000282, 000284, 000287, 000288, 000289, 000290, 000292, 000294, 000295, 000297, 000299, 000300, 000302, 000304, 000306, 000307, 000309, 000310, 000311, 000314, 000316, 000321, 000322, 000323, 000324, 000325, 000330, 000332, 000334, 000335, 000337, 000

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0026-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.