Home › Device types › GNC
Antigens, Febrile, Slide And Tube, All Groups, Salmonella Spp.
FDA product code GNC · Class 2 · Microbiology
297
Registered devices
0
Adverse events
5
Recalls
60
510(k) clearances
Devices with this code
Vision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDNA — REMEL EUROPE LIMITEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATEDVision 2 — PRO-LAB, INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-05-19 | Becton Dickinson & Co. | In vitro diagnostic reagent to aid in the diagnosis of Salmonellosis may exhibit decreased or no reactivity. If proper controls are run with the lot in question |
| 2004-10-20 | BD Diagnostic Systems | Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions. |
| 2004-10-20 | BD Diagnostic Systems | Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions. |
| 2004-10-20 | BD Diagnostic Systems | Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions. |
| 2004-10-20 | BD Diagnostic Systems | Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions. |
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.