Becton Dickinson & Co.: Medical Device Recall in 2022 - (Recall #: Z-1018-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 9, 2022

Date Posted: May 11, 2022

Recall Number: Z-1018-2022

Event ID: 89896

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.

Status: Terminated

Product Quantity: 15 systems

Code Information:

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

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated