ClearanceBrief
Recall Z-0653-2021 ยท DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

CryoLife, Inc.

CryoPatch SG Pulmonary Human Cardiac Patch. The patch 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 patch into the operating environment. Supercooling by liquid nitrogen boost is begun prior to cryst

DateNov 10, 2020
StatusTerminated
ReasonOn 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.
Root causeMaterial/Component Contamination
ActionA Recall notification letter titled "Urgent - Voluntary Human Tissue Recall" was sent to consignees via email or hand delivered by firm representatives. On 11-Nov-2020, 4 letters were delivered to consignees. On 12-Nov-2020, 2 letters were delivered to consignees. The letter instructs the consignee to complete and return the enclosed postcard affirming that they received the notification. The affected product should be quarantined and returned to CryoLife immediately, if it has not been implanted. CryoLife Field Representatives were to provide information necessary to arrange for the return of
Quantity2 units
DistributionDistributed nationwide to GA, AZ, TX, MO, and OK.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K101866CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH
Cryolife, Inc., Jul 23, 2010