FEMSelect Ltd: Medical Device Recalls in 2022

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by FEMSelect Ltd in 2022. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

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.