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Recall Observatory FDA recall evidence

Device product

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.

Z-2073-2023

May 23, 2023

Class II

Product summary

Firm
TEI Biosciences, Inc.
Event
Event 92481
Status
Ongoing
Classification
Class II
Quantity
3,992 units
Official record key
device-enforcement:Z-2073-2023

Official wording

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

Code information: Item No. (UDI-DI): 606-206-001 (10381780357339), 606-206-002 (10381780357360), 606-206-003 (10381780357346), 606-206-004 (10381780357353), 606-206-005 (10381780357377), 606-206-006 (10381780357384), and 606-206-007 (10381780357391).

Distribution pattern: Domestic: Nationwide Distribution.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out of specification