FDAJune 22, 2022device

Crome Implantable Cardioverter Defibrillators: a. Crome VR ICD, Model Numbers: DVPC3D1, DVPC3D4; b. Crome DR ICD, Model Numbers: DDPC3D1, DDPC3D4

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

The hazard

There is the potential for reduced shock energy (~79% of programmed energy) during high-voltage (HV) therapy for Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).

What to do

FDA enforcement status: Ongoing

Brands named

medtronic inc cardiac rhythm and heart failure crhfmedtronicmedtronic inc

UPCs

00763000178543007630001785500076300017856700763000178413007630001784200076300017843700763000178444

Recall history

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

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