FDAJanuary 25, 2022device

CoolSeal Generator, REF: CSL-200-50

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

The hazard

A potential manufacturing/assembly defect could result in the generator not meeting IEC 60601 standards for medical electrical equipment, and it can potentially, under specific conditions, lead to the delivery of unintended energy to the patient.

What to do

FDA enforcement status: Terminated

Brands named

bolder surgicalbolder

UPCs

00850346007023

Recall history

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

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