Health product recall

Ysio Max, Luminos dRF Max, and Uroskop Omnia Max (2018-12-11)

Starting date:
December 11, 2018
Posting date:
January 9, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-68654

Affected products

  1. Ysio Max
  2. Luminos dRF Max
  3. Uroskop Omnia Max

Reason

Software update VF10C provides various bug fixes to correct respective bugs and prevents them from recurring.

Affected products

A. Ysio Max

Lot or serial number

27053
27054
27055
27058
27061
27070
27071
27089
27090
27092
27097

Model or catalog number

10762470

Companies
Manufacturer
Siemens Healthcare GmbH
Henkestr. 127
Erlangen
91052
GERMANY

B. Luminos dRF Max

Lot or serial number

7011
7037
7044
7046
7049
7060
7067
7100
7102
7132
7167

Model or catalog number

10762471

Companies
Manufacturer
Siemens Healthcare GmbH
Henkestr. 127
Erlangen
91052
GERMANY

C. Uroskop Omnia Max

Lot or serial number

5034
5041

Model or catalog number

10762473

Companies
Manufacturer
Siemens Healthcare GmbH
Henkestr. 127
Erlangen
91052
GERMANY