RecallRadar

FDA Device recall Z-1018-2022

BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10

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

AgencyFDA Device
Recall numberZ-1018-2022
ClassificationClass II
Statusterminated
Initiated2022-03-09
Published2022-05-11
Last updated2026-09-13 11:56 UTC
CompanyBecton Dickinson And
DistributionUS

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

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.