Becton Dickinson & Co.: Medical Device Recall in 2019 - (Recall #: Z-2438-2019)

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: 447202

Product Classification:

Class II

Date Initiated: July 26, 2019

Date Posted: September 11, 2019

Recall Number: Z-2438-2019

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: 4 units

Code Information:

Catalog Number: 447202 Catalog Number/UDI INO-000287 00382904472023 INO-000286 00382904472023 INO-000269 00382904472023 INO-000281 00382904472023

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated