Reported Oct 16, 2019 · Terminated
BD FACSLyric Flow Cytometer,3-Laser 10 Color Instrument, REF: 659180 and 65918001, when using BD Trucount Tubes
Becton, Dickinson and Company, BD Biosciences
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 and Company, BD Biosciences · 2350 Qume Dr · San Jose, CA · 95131-1812
Is this the product you have?
- BD FACSLyric Flow Cytometer,3-Laser 10 Color Instrument
- REF659180 and 65918001, when using BD Trucount Tubes
- Lot codes and dates
- BD
- FACSLyric Flow Cytometer serial numbers
237 of 237 codes
9180000057918000021991800002830000001R6591800R658180000282R6591800000082R6591800000083R659180000045R659180000051R659180000061R659180000063R659180000064R659180000068R659180000071R659180000075R659180000089R659180000099R659180000137R659180000167R659180000196R659180000202R659180000204R659180000211R659180000213R659180000229R659180000230R659180000231R659180000232R659180000233R659180000234R659180000235R659180000236R659180000237R659180000239R659180000240R659180000241R659180000242R659180000243R659180000244R659180000245R659180000246R659180000247R659180000248R659180000249R659180000250R659180000251R659180000252R659180000253R659180000254R659180000255R659180000256R659180000257R659180000258R659180000259R659180000260R659180000261R659180000262R659180000263R659180000264R659180000265
- Amount recalled
- 236
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
Why it was recalled
Flow cytometers, when used with specific tubes may experience excessive electronic abort counts (electronic abort count of beads exceeds 1.0% of the total processed events), which may affect the ratio of cell population events to bead events, potentially resulting in falsely high absolute counts. This may affect the following: initiation of prophylactic therapy for Opportunistic Infections (HIV patients), decisions regarding care/management (PID/immune suppressed patients), laboratory developed tests/experiments, specimen engraftment potency, and use of leucoreduced blood products for transfusion.
This product could cause temporary or reversible health problems — stop using it.
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