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