PlainRecalls
FDA Devices Moderate Class II Ongoing

PriMatrix Ag; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.

Reported: July 12, 2023 Initiated: May 23, 2023 #Z-2080-2023

Product Description

PriMatrix Ag; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.

Reason for Recall

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

Details

Recalling Firm
TEI Biosciences, Inc.
Units Affected
1,689 units
Distribution
Domestic: Nationwide Distribution.
Location
Boston, MA

Frequently Asked Questions

What product was recalled?
PriMatrix Ag; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.. Recalled by TEI Biosciences, Inc.. Units affected: 1,689 units.
Why was this product recalled?
Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 12, 2023. Severity: Moderate. Recall number: Z-2080-2023.