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BD Phoenix™ NID
BECTON, DICKINSON AND COMPANY · Model 448007 · UDI-DI 00382904480073
LQM
Prescription
7
510(k) clearances
388
Adverse events (2 deaths)
2
Recalls
11
Facilities
Description
BD Phoenix™ NID
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-11-09 | Biomerieux Inc | As the temperature and time out of range was exceeded, product performances cannot be guaranteed |
| 2017-04-20 | Biomerieux Inc | The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency). |
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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.