FDADecember 12, 2024device

VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)

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

The hazard

A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

0080252655938900802526559396008025265771090080252657879300802526577024008025265594020080252655941900802526576522008025265781200080252657703100802526593284

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128) — Recall Details · AllClear