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FDA Medical Device Recalls (openFDA)

Siemens Medical Solutions, USA, Inc: Siemens Medical Solutions, syngo Dynamics 6.0 Workplace; Picture archiving and communication system

Recall number
Z-1751-2008
Recalling firm
Siemens Medical Solutions, USA, Inc
Product
Siemens Medical Solutions, syngo Dynamics 6.0 Workplace; Picture archiving and communication system
Status
Terminated
Initiated
2008-02-08
Posted
2008-09-29
Terminated
2009-11-18
Reason
Incorrect data: A software bug may result in a transfer of patient demographic data to a different patient's file.
Root cause
Software design
Action
Siemens issued a customer safety advisory to users on 2/8/08 advising them of the problem and instructing them to complete and verify that the report is locked before opening and reporting on a second patient, and that a software patch will be available Spring 2008.
Quantity
18
Distribution
Nationwide Distribution: Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Michigan, Missouri, Montana, North Carolina, Texas and Utah.
Lot, serial or model codes
All units with version 6.0 software.
510(k) numbers
["K070322"]
PMA numbers
not on file
Product code
LLZ
Firm FEI
3003304172
Firm city
Ann Arbor
Firm state
MI
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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