Device recall
Z-0198-2018: BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed…
FDA device recall · Class III · Becton Dickinson & Co.
Key facts
| Recall number (Z-number) | Z-0198-2018 |
|---|---|
| Recall event | 78102 |
| Product | BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples… |
| Product code | JQX |
| Recalling firm | Becton Dickinson & Co. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 9, 2018 |
| FEI number | 1119779 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database