Home › Device types › LGB
Gonococcal Antibody Tests
FDA product code LGB · Class 3 · Microbiology
0
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-05-26 | Pall Corporation | Potential for the housing of the arterial line Leukocyte Reduction Filter to separate before or during the priming procedure. |
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