FDA Device Intelligence
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

DateFirmReason
2022-11-09Biomerieux IncAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
2022-11-09Biomerieux IncAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
2022-11-09Biomerieux IncAs 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 docs
Data 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.