Health product recall

Ysio Max, Luminos DRF Max & Uroskop Omnia Max (2020-04-27)

Starting date:
April 27, 2020
Posting date:
May 8, 2020
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-73035



Last updated: 2020-05-08

Affected Products

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

Reason

Update of system version VF10E_HF02 to VF10F to provide various bug fixes and to prevent them from recurring.

Affected products

A. Ysio Max

Lot or serial number
  • 27622
  • 27729
  • 27793
Model or catalog number
  • 10762470
Companies
Manufacturer

Siemens Healthcare GMBH

Henkestr. 127

Erlangen

91052

GERMANY


B. Luminos DRF Max

Lot or serial number
  • 7588
Model or catalog number
  • 10762471
Companies
Manufacturer

Siemens Healthcare GMBH

Henkestr. 127

Erlangen

91052

GERMANY


C. Uroskop Omnia Max

Lot or serial number
  • 5151
  • 5148
Model or catalog number
  • 10762473
Companies
Manufacturer

Siemens Healthcare GMBH

Henkestr. 127

Erlangen

91052

GERMANY