FDAJanuary 22, 2020device

Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C (05414734507585), CD1277-36 (05414734506045), CD1377-36C (05414734507622), CD2277-36Q (05414734505932), CD2377-36QC (05414734507523), with Merlin Patient Care System with software model 3330

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Past updates to programmers and transmitters may lead some implantable cardioverter defibrillators (ICD) to lose wireless radiofrequency (RF) communication; which means patients can no longer be interrogated with wireless RF telemetry or monitored remotely.

What to do

FDA enforcement status: Terminated

Brands named

st jude medical cardiac rhythm management division

UPCs

054147345076460541473450758505414734506045054147345076220541473450593205414734507523

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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