FDA recall Z-0172-2020

MEDTECH SAS · Class I · device

Product

Rosa Brain 3.0, Model No. ROSA 3.0. The device is delivered assembled in a wooden case and protected with plastic bubble and plastic film. Seals are put on the crate. The product is not shipped sterile. The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons.

Reason for recall

The instrument holder may be sent on a trajectory that is not within the intended target. If it is not corrected, the associated device may be placed incorrectly.

Distribution

Nationwide domestic distribution. Foreign distribution to Australia, France, Switzerland, Taiwan, and Vietnam.

Key facts

Status
Terminated
Initiation date
2019-09-10
Report date
2019-11-13
Termination date
2021-11-02
Voluntary/Mandated
Voluntary: Firm initiated
Location
Montpellier, N/A, France

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0172-2020