This page has been archived on the Web

Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.

Health product recall

ROSA (2017-09-15)

Starting date:
September 15, 2017
Posting date:
November 22, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Hospitals, Healthcare Professionals
Identification number:
RA-65182

Affected products

ROSA

Reason

It has been identified that early wear and tear of the articulated arm may occur, which could cause instability of the articulated arm during surgery, potentially leading to undetected patient head motion.

Affected products

ROSA

Lot or serial number

RO10010
RO14030

Model or catalog number

RO

Companies
Manufacturer
MEDTECH S.A
ZAC EUREKA
900 RUE DU MAS DE VERCHANT
MONPELLIER
34000
FRANCE