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Recall Observatory FDA recall evidence

Device product

syngo(R) Lab Data Manager and syngo(R) Lab Process Manager, all versions. This device is classified as a data calculator and processing module for use with In-vitro diagnostic devices. It also provides work flow management as well as remote instrument control to multiple interfaced instruments.

Z-2305-2012

May 29, 2012

Class II

Product summary

Firm
Siemens Healthcare Diagnostics, Inc.
Event
Event 62709
Status
Terminated
Classification
Class II
Quantity
44
Official record key
device-enforcement:Z-2305-2012

Official wording

Reason: When using the syngo Quality Control package the system may not perform as intended for Multi-Rule QC violation [e.g., 2(2S), 4(1s) and 10x], unless configured using the instructions on page 2 of the recall notification. QC status may not be flagged appropriately. If auto-verification rules are defined to hold patient results when QC status is out, the patient results will not be held as expecte

Code information: Version VA11B and all previously released versions.

Distribution pattern: USA ( nationwide ) including the states of AZ, CA, FL, IL, KY, MD, MA, MN, MS, MO, NE, NH, NJ, NY, NC, OH, PA, TX, VA and WV.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    When using the syngo Quality Control package the system may not perform as intended for Multi-Rule QC violation [e.g., 2(2S), 4(1s) and 10x], unless configured using the instructions on page 2 of the recall notification. QC status may not be flagged appropriately. If auto-verification rules are defined to hold patient results when QC status is out, the patient results will not be held as expecte