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ACell, Inc recalls Gentrix Surgical Matrix Thick, 20 x 30cm, Catalog Number PSMT2030, Lot 013948 - Product Usage: Gentrix Surgical Matrix T
Recalled March 27, 2019 · FDA recall Z-1033-2019 · ACell
Hazard
The devices were released from a lot for which one sample failed to meet the company' s tensile strength specification for lot release. · FDA Class II
Units
1
Sold at
US nationwide distribution in the state of CA.
Description
The devices were released from a lot for which one sample failed to meet the company' s tensile strength specification for lot release.
Product
Gentrix Surgical Matrix Thick, 20 x 30cm, Catalog Number PSMT2030, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive surgery. Reinforcement of soft tissue within gastroenterological and plastic & reconstructive surgery includes, but is not limited to the following procedures: hernia and body wall repair, colon and rectal prolapse repair, tissue repair, and esophageal repair.
Manufacturer(s)
ACell, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →