PlainRecalls
FDA Devices Moderate Class II Terminated

BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202

Reported: September 11, 2019 Initiated: July 26, 2019 #Z-2438-2019

Product Description

BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202

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

Details

Recalling Firm
Becton Dickinson & Co.
Units Affected
4 units
Distribution
Illinois, Iowa, Missouri, New York, Ohio, Tennessee World Wide (5): Singapore, Taiwan, France, Netherlands
Location
Sparks, MD

Frequently Asked Questions

What product was recalled?
BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202. Recalled by Becton Dickinson & Co.. Units affected: 4 units.
Why was this product recalled?
An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate
Which agency issued this recall?
This recall was issued by the FDA Devices on September 11, 2019. Severity: Moderate. Recall number: Z-2438-2019.