FDAMay 14, 2018device

Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020

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

The hazard

Devices, which met FDA and AATB eligibility criteria, were distributed. Final autopsy and toxicology reports indicated the presence of morphine in the urine.

What to do

FDA enforcement status: Terminated

Brands named

cryolife

Recall history

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

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