Z-0814-2007

BacT/VIEW Software, all versions. in vitro diagnostic database software

Name: Z-0814-2007 BacT/VIEW Software, all versions. in vitro diagnostic database software
Creator: bioMerieux, Inc.
Published: 2006-12-19
License: https://open.fda.gov/license/

bioMerieux, Inc. / initiated 2006-12-19 / Terminated

FDA source

bioMerieux, Inc. began a recall of BacT/VIEW Software, all versions. in vitro diagnostic database software on 2006-12-19. The reason FDA records is "BacT/VIEW will be unable to run scheduled macro applications unless the user touches the BacT/VIEW touch screen or clicks a function after resynchronizing the clocks". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0814-2007
Status: Terminated
Initiated: 2006-12-19
Posted: 2007-05-18
Terminated: 2009-12-08
Recalling firm: bioMerieux, Inc.
Product: BacT/VIEW Software, all versions. in vitro diagnostic database software.
Product code: MDB System, Blood Culturing
Reason for recall: BacT/VIEW will be unable to run scheduled macro applications unless the user touches the BacT/VIEW touch screen or clicks a function after resynchronizing the clocks.
FDA root cause: Other
Action: A customer notification was sent on/about December 19, 2006. Customers will be sent a new BacT/VIEW software version C.30b QTR 1 2007.
Quantity in commerce: 1233 units
Distribution: Worldwide, including USA, Canada, UK, Italy, France, Spain, Germany, Poland, Chile, Japan and the Netherlands.
Product codes and lots: Product Numbers: Software Version C.30a -22105-68, Update Disk; 22105-69 Install Disk

Product code MDB

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)