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BioPlex 2200
BIO-RAD LABORATORIES, INC. · Model 6632440 · UDI-DI 00847865000758
3
510(k) clearances
0
Adverse events
1
Recalls
2
Facilities
Description
MMRV IgG Control Lot Data
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-05-05 | Cell Marque Corporation | Cell Marque has determined the need to issue a product recall after identifying product intended to be sold outside the U.S. was not properly labeled as "For Export Only" as requir |
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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.