Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner pouch seal may be inadequate resulting in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ProgenaCare directly.
Affected Products
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.
Quantity: 547 packages
Why Was This Recalled?
Inner pouch seal may be inadequate resulting in lack of sterility.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ProgenaCare
ProgenaCare has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report