FDA Device recall Z-1018-2022
BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10
- FDA Device
- Class II
- terminated
- Published 2022-05-11
On 2022-05-11 the FDA classified a Class II recall of BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10 by Becton Dickinson And, citing when updating BD Kiestra customers to BD Synapsys version 4.10, the custom antibiotic codes set by the customer are overwritten with the BD default antibiotic codes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1018-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-03-09 |
| Published | 2022-05-11 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10
Reason
When updating BD Kiestra customers to BD Synapsys version 4.10, the custom antibiotic codes set by the customer are overwritten with the BD default antibiotic codes.
Identifiers
| code_info | All systems running BD Synapsys version 4.10; UDI: 00382904441500; Serial Numbers: SL00530 SL00515 SL00527 SL00502 SL…All systems running BD Synapsys version 4.10; UDI: 00382904441500; Serial Numbers: SL00530 SL00515 SL00527 SL00502 SL00540 SL00564 SL00549 SL00509 SL00003 SL00004 SL00010 SL00001 SL00005 SL00002 SL000015 SL01010 SL01022 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1018-2022%22
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