BD FACSLyric 662876Recalls & reported problems
Becton, Dickinson And Company · BD FACSLyric™ Flow Cytometer · Class 2
All models of BD FACSLyric (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Nov 1, 2024Class IIOpen, Classified
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W 12/24V M3S4S6) on BD FACSLyric flow cytometers, which has the potential for the instruments to fail to power on and/or stay on. The potential power supply failure on BD FACSLyric Flow Cytometer may lead to risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. The patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In addition, patient specimen loss and/ or delay providing results of testing results. There may be additional risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. In addition, the patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In the Notification Letter sent on November 20, 2024, customers are instructed to continue their normal operation of your BD FACSLyric Flow Cytometer according to the Instructions For Use after immediately inspecting inventory for the specific catalog and power supply serial numbers listed in the notification letter and follow the instructions listed under Actions for Clinical Users.
Z-0746-2025 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other Flow cytometric reagents and accessories. devices
- FACSCanto 338962Becton, Dickinson And Company · Flow cytometric reagents and accessories.167 reports
- BD FACSLyric 662878Becton, Dickinson And Company · Flow cytometric reagents and accessories.2 recalls23 reports
- FACSLyric 663518Becton, Dickinson And Company · Flow cytometric reagents and accessories.1 recall65 reports
- BD FACSLyric 662875Becton, Dickinson And Company · Flow cytometric reagents and accessories.1 recall10 reports
- BD FACSLyric 662877Becton, Dickinson And Company · Flow cytometric reagents and accessories.1 recall1 report
- DxFLEX C78500Beckman Coulter, Inc. · Flow Cytometric Reagents And Accessories.1 recall0 reports
- FACS 662879Becton, Dickinson And Company · Flow cytometric reagents and accessories.1 recall0 reports
- FACSCanto 657338Becton, Dickinson And Company · Flow cytometric reagents and accessories.46 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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