PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: May 11, 2022 Initiated: March 9, 2022 #Z-1018-2022

Product Description

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

Reason for Recall

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.

Details

Recalling Firm
Becton Dickinson & Co.
Units Affected
15 systems
Distribution
Worldwide distribution US Nationwide distribution in the states of CA, IL, MI, NY, OH, SC, and TN. The countries of Austria, France, Germany, Netherlands, Sweden.
Location
Sparks, MD

Frequently Asked Questions

What product was recalled?
BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10. Recalled by Becton Dickinson & Co.. Units affected: 15 systems.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 11, 2022. Severity: Moderate. Recall number: Z-1018-2022.