Becton Dickinson & Co.: Medical Device Recall in 2019 - (Recall #: Z-2439-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing Catalog Number : 447213

Product Classification:

Class II

Date Initiated: July 26, 2019

Date Posted: September 11, 2019

Recall Number: Z-2439-2019

Event ID: 83513

Reason for Recall:

An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate

Status: Terminated

Product Quantity: 9 units

Code Information:

Catalog Number: 447213 Serial Number/UDI: INO-000290 00382904472139 INO-000263 00382904472139 INO-000264 00382904472139 20130276 00382904472139 INO-000282 00382904472139 INO-000284 00382904472139 INO-000272 00382904472139 INO-000274 00382904472139

Distribution Pattern:

Illinois, Iowa, Missouri, New York, Ohio, Tennessee World Wide (5): Singapore, Taiwan, France, Netherlands

Voluntary or Mandated:

Voluntary: Firm initiated