Home › BECTON, DICKINSON AND COMPANY › BD Francisella Tularensis Antiserum
BD Francisella Tularensis Antiserum
BECTON, DICKINSON AND COMPANY · Model 240939 · UDI-DI 00382902409397
GSK
Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
1
Facilities
Description
Vial F Tularensis Antiserum
Recalls
| Date | Firm | Reason |
|---|---|---|
| 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 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.