ProgenaCare Recall: progenamatrix Human Keratin Matrix, sterile, Rx, with the following mo
ProgenaCare Recall: progenamatrix Human Keratin Matrix, sterile, Rx, with the following mo is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: ProgenaCare; Product: progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1) PM2012, 12 x 2 cm; (2) PM3002, 2 x 2 c
| Recalling firm | ProgenaCare |
|---|---|
| Product | 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. |
| Reason for recall | Inner pouch seal may be inadequate resulting in lack of sterility. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide distribution in the states of AL, GA, FL, TN, and TX. There was no foreign/military/government distribution. |
| Recall initiated | 20220418 |
| Recall number | Z-1137-2022 |
| Category | device |
| State | GA |
| Country | United States |
$29/mo
Try RecallGuard →