FDA Device recall Z-0198-2018
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standar…
- FDA Device
- Class III
- terminated
- Published 2017-12-13
On 2017-12-13 the FDA classified a Class III recall of BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standar… by Becton Dickinson And, citing potential unexpected movement of robot arm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0198-2018 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-06-01 |
| Published | 2017-12-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Becton Dickinson And |
| Distribution | CA, NC, TN |
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 for use on the BD Phoenix" system, which performs identification and susceptibility testing
Reason
Potential unexpected movement of robot arm
Identifiers
| code_info | Serial Numbers: AP0447, AP0448, AP0449, AP0450, AP0451, AP0458 & AP0463. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0198-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.