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Cobas IT 1000 Software (2014-07-24)
- Starting date:
- July 24, 2014
- Posting date:
- August 8, 2014
- 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-40843
Recalled products
- Cobas IT 1000 Software
Reason
A potential issue observed when the Cobas IT 1000 receives an ADT admit, merge or transfer event message that contains a genuine patient ID which is the same as what has been configured in Cobas IT1000 as the generic patient ID.
Affected products
A. Cobas IT 1000 Software
Lot or serial number
- Versions 2.01.00 to 2.03.00
Model or catalog number
- 04420306001
- 04481763001
Companies
- Manufacturer
-
Roche Diagnostics GmbH
Sandhofer Strasse 116
Mannheim
68305
GERMANY