FDAClass IIDecember 30, 2020

CryoValve SG Pulmonary Human Heart Valve. The valve is recall: Contamination

CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing cryoprotectants within the innermost pouch…

Why was CryoValve SG Pulmonary Human Heart Valve. The valve is recalled?

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 should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model/Catalog Number: SGPV00 Serial Numbers: 11685214, 11685554, and 11682491 UDI: 00877234000447

Product
CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing cryoprotectants within the innermost pouch…
Recalling firm
CryoLife, Inc.
Quantity
3 units
Distribution
Distributed nationwide to GA, AZ, TX, MO, and OK.
Recall date
December 30, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
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