TEI Biosciences recalls SurgiMend MP collagen matrix products due to potential endotoxin test failures. These products are prescription-only and used for soft tissue reconstruction. Consumers should contact the manufacturer for details.
Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
TEI Biosciences is recalling SurgiMend MP collagen matrix products for soft tissue reconstruction because of possible issues with endotoxin testing. This could affect the safety of the product when used in medical procedures.
The recall is due to possible out of specification endotoxin test results. Endotoxins are bacterial components that can cause serious infections if present in medical products. The issue may arise from problems in testing during manufacturing.
Prescription patients using SurgiMend MP for soft tissue reconstruction are affected. Medical professionals who use these products are at the highest risk.
Check for the product names SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only. Look for specific sizes: 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm. The item numbers are 606-206-001 through 606-206-007.
Reach out to TEI Biosciences for specific details about the recalled products and next steps.
The recall indicates possible endotoxin test issues, but the product may still be safe. Contact TEI Biosciences for clarification.
The recall does not specify a remedy, so contact TEI Biosciences for instructions.
Yes, check for sizes: 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm. Item numbers are 606-206-001 through 606-206-007.
We’ve drafted a message you can send TEI Biosciences to request your refund or repair — edit it as you like.
Subject: Recall Z-2073-2023 — TEI Biosciences TEI Biosciences Hello, I own a TEI Biosciences that is covered by recall Z-2073-2023 from TEI Biosciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
