Home › Device types › MLA
Dna Probe, Yeast
FDA product code MLA · Class 1 · Microbiology
6
Registered devices
190
Adverse events
2
Recalls
2
510(k) clearances
Devices with this code
CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCBD Affirm™ VPIII Microbial Identification Test — BECTON, DICKINSON AND COMPANYCARDINAL HEALTH — Cardinal Health 200, LLCBD Affirm™ VPIII Microbial Identification Test — BECTON, DICKINSON AND COMPANY
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-08-27 | Becton Dickinson & Co. | BD has confirmed that a portion of tests associated with the affected lots( 446252 and 446257 ) of product may exhibit blue speckles or fibers on the beads and |
| 2013-06-13 | Becton Dickinson & Co. | In vitro diagnostic test kit may exhibit invalid internal negative control results. |
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.