Reported Sep 11, 2019 · Terminated
BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing Catalog Number : 447213
Becton Dickinson & Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- BD Kiestra InoqulA+ Software Version 20.3. IVD automated
- specimen processing Catalog Number447213
- Lot codes and dates
- Catalog Number447213
- Serial Number/UDI
INO-00029000382904472139INO-00026300382904472139INO-000264003829044721392013027600382904472139INO-00028200382904472139INO-00028400382904472139INO-00027200382904472139INO-00027400382904472139
- Amount recalled
- 9 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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