FDAMarch 15, 2022device

CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US

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

The hazard

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c. when used with a defibrillator at a voltage above its maximum threshold, Claravue does not meet the specification and delivers an inefficient electrical charge which may result in an ineffective defibrillation.

What to do

FDA enforcement status: Terminated

Brands named

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UPCs

037005063073023202878150604

Recall history

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

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CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US — Recall Details · AllClear