Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1018-2022 — BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10

U.S. FDA — Device Enforcement · United States · 2022-03-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1018-2022
Date of alert
2022-03-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Co.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00382904441500
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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