Home › Device types › GRO
Antisera, Fluorescent, All Types, Hemophilus Spp.
FDA product code GRO · Class 2 · Microbiology
0
Registered devices
0
Adverse events
1
Recalls
4
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-10-22 | Becton Dickinson & Co. | In vitro diagnostic test kit was not manufactured according to specifications and may cause false negatives or misidentification of Hemophilus species present i |
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