[Recalled] BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number 662878 BD FACSLyric is a high-performance flow cytometer designed to support both routine clinical analysis and research for the identification, quanti
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number 662878 BD FACSLyric is a high-performance flow cytometer designed to support both routine clinical analysis and research for the identification, quantification, and characterization of cells in support of cell analysis. BD |
|---|---|
| Brand / manufacturer | Becton, Dickinson and Company, BD Biosciences |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0792-2019 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 02 January 2019 |
| EAN / barcode | 00382906628787 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: A customer site was identified to have three FACSLyric IVD systems with FACSuite clinical v1.1.1 installed on a computer workstation with windows 10 operating system (OS). Windows 10 OS is not a released configuration for clinical use. It is released for research use only.
This Class III recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.