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FDA (Device enforcement)Recalled 2023-05-23class ii

TEI Biosciences, Inc.: PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18mm Disc, 2x2 cm, and 10x25 cm (Meshed 2:1).

Hazard

Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.

Details from the source

Reason for recall: Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing. Distribution: Domestic: Nationwide Distribution. Quantity: 30,528 units Lot/code info: Item No. (UDI-DI): 607-004-440 (10381780113379), 607-004-660 (10381780113386), 607-004-880 (10381780113393), 607-005-014 (10381780357414), 607-005-018 (10381780357421), 607-005-125 (10381780113409), 607-005-220 (10381780357407).

UPC codes

10381780113379, 10381780113386, 10381780113393, 10381780357414, 10381780357421, 10381780113409, 10381780357407

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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