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

Recall Z-2081-2023 — PriMatrix Ag Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.

U.S. FDA — Device Enforcement · United States · 2023-05-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2081-2023
Date of alert
2023-05-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
TEI Biosciences, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10381780113775
Reported risk: Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.