FDA recall Z-2118-2020

Clinical Innovations, LLC · Class II · device

Product

Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOTAL, 7 cm* * *CLINICAL INNOVATIONS Manufacturer: Clinical Innovations, LLC* * *Reorder Number: UM750* * *LOT 181183* * *." Each device is accompanied by Instruction for Use which is similarly labeled.

Reason for recall

An incorrect component used during manufacturing. The uterine manipulator tip support does not have the "notch" required to attach the spacer and or colpotomy cup. This may result in a delay in surgery and additional surgical interventions to completed the procedure. There was a report of an injury.

Distribution

International distribution to the country Japan.

Key facts

Status
Terminated
Initiation date
2019-05-30
Report date
2020-06-03
Termination date
2020-08-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Murray, UT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2118-2020