FDANovember 10, 2020device

CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing cryoprotectants within the innermost pouch of a three-pouch packaging system. The packaging system not only withstands ultracold temperatures, but also allows for aseptic introduction of the...

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

The hazard

On November 10, 2020, it was discovered that there are post- processing microbial culture test failures for other allografts, processed using a TRIS saline solution lot that was also used in processing allografts subjected to the recall.

What to do

FDA enforcement status: Terminated

Brands named

cryolife

UPCs

00877234000447

Recall history

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

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CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing cryoprotectants within the innermost pouch of a three-pouch packaging system. The packaging system not only withstands ultracold temperatures, but also allows for aseptic introduction of the... — Recall Details · AllClear