FDA Device recall Z-1200-2017
VIDAS 3 software v. 1.1.4
- FDA Device
- Class II
- terminated
- Published 2017-02-22
On 2017-02-22 the FDA classified a Class II recall of VIDAS 3 software v. 1.1.4 by Biomerieux, citing during development of the VIDAS 3 software version 1.2, some anomalies have been identified and observed to be already present in the current software version VIDAS 3 version 1.1.….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1200-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-11 |
| Published | 2017-02-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Biomerieux |
| Distribution | n/a |
Product
VIDAS 3 software v. 1.1.4
Reason
During development of the VIDAS 3 software version 1.2, some anomalies have been identified and observed to be already present in the current software version VIDAS 3 version 1.1.4. available in the field.
Identifiers
| code_info | REF: #412590, Lot: Software version 1.1.4 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1200-2017%22
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