Home › BIOMERIEUX SA › VITEK®MS
VITEK®MS
BIOMERIEUX SA · Model VITEKMS SW v1.0 / FlexPrep v1.0 · UDI-DI 03573026610418
PEX
Prescription
2
510(k) clearances
431
Adverse events
3
Recalls
7
Facilities
Description
DVD to install VITEK MS SW v1.0 and VITEK MS FlexPrep v1.0 for clinical customers
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-11-09 | Biomerieux Inc | As the temperature and time out of range was exceeded, product performances cannot be guaranteed |
| 2022-11-09 | Biomerieux Inc | As the temperature and time out of range was exceeded, product performances cannot be guaranteed |
| 2022-11-09 | Biomerieux Inc | As the temperature and time out of range was exceeded, product performances cannot be guaranteed |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
