BD Kiestra InoqulA Software Version 20.3.IVD automated recall: Software Issue
BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202
Why was BD Kiestra InoqulA Software Version 20.3.IVD automated recalled?
An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog Number: 447202 Catalog Number/UDI INO-000287 00382904472023 INO-000286 00382904472023 INO-000269 00382904472023 INO-000281 00382904472023
- Product
- BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202
- Recalling firm
- Becton Dickinson & Co.
- Quantity
- 4 units
- Distribution
- Illinois, Iowa, Missouri, New York, Ohio, Tennessee World Wide (5): Singapore, Taiwan, France, Netherlands
- Recall date
- September 11, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)