FACS 662879Recalls & reported problems
Becton, Dickinson And Company · BD FACS™ Universal Loader · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 16, 2018Terminated
The solenoid plunger tip length is too short resulting in insufficient engagement to the Universal Loader enclosure to lock during use.
Z-2598-2018 · Root cause: Nonconforming Material/Component · 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
- BD FACSLyric 662876Becton, 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 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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