FDA recall Z-0556-2022

FEMSelect Ltd · Class II · device

Product

The EnPlace is a single use trans-vaginal pelvic floor repair system which enables delivery of a tissue anchor to the ligaments of the vaginal cavity. The anchors are pre-loaded inside the device shaft and are ready for use. A thimble is also supplied, as an accessory for the device, to be used as a guide channel for better handling of the EnPlace. Intended Use / Indications for Use: The EnPlace system is intended for attaching sutures to ligaments of the pelvic floor.

Reason for recall

Certain lots may not have been packaged wth the Channel Tube Limiter.

Distribution

US Nationwide distribution in the state of Georgia.

Key facts

Status
Ongoing
Initiation date
2021-12-13
Report date
2022-02-09
Voluntary/Mandated
Voluntary: Firm initiated
Location
Modi'in, N/A, Israel

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0556-2022