PlainRecalls
FDA Devices Moderate Class II Ongoing

SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm.

Reported: July 12, 2023 Initiated: May 23, 2023 #Z-2073-2023

Product Description

SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 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
3,992 units
Distribution
Domestic: Nationwide Distribution.
Location
Boston, MA

Frequently Asked Questions

What product was recalled?
SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm.. Recalled by TEI Biosciences, Inc.. Units affected: 3,992 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-2073-2023.