Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1137-2022 — progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1) PM2012, 12 x 2 cm; (2) PM3002, 2 x 2 cm; (3) PM3004, 4 x 4 cm; PM3006, 6 x 6 cm; and PM3010, 10 x 10 cm.

U.S. FDA — Device Enforcement · United States · 2022-04-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1137-2022
Date of alert
2022-04-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ProgenaCare
Product category
device
Product type
Devices
Reported risk: Inner pouch seal may be inadequate resulting in lack of sterility.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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