Health product recall

SYNGO DYNAMICS (2020-10-27)

Starting date:
October 27, 2020
Posting date:
November 13, 2020
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-74291



Last updated:
2020-11-13

Affected Products

SYNGO DYNAMICS

Reason

Bug fixing and improvements for software addressing the following defects:

  • When study is in progress sending the SR or creating a fetus in SD worksheet, data between multiple fetuses are being mixed together, omitted, or duplicated.
  • VA20F fixup tool still completes fixup and merges study even if clicking ""X"" in upper corner on the possible merge dialog box.
  • Misconfiguration of the syngo Dynamics product allowed approximately 500 legacy studies to be deleted from the SD database.

Affected products

SYNGO DYNAMICS

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

VA20

Companies
Manufacturer

Siemens Healthcare GMBH

Henkestr. 127

Erlangen

91052

GERMANY