FDA recall Z-1032-2019

ACell, Inc · Class II · device

Product

Gentrix Surgical Matrix Thick, 30 x 40cm, Catalog Number PSMT3040, 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.

Reason for recall

The devices were released from a lot for which one sample failed to meet the company' s tensile strength specification for lot release.

Distribution

US nationwide distribution in the state of CA.

Key facts

Status
Terminated
Initiation date
2019-02-14
Report date
2019-03-27
Termination date
2020-05-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Columbia, MD, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1032-2019