BD Multi-Check 349705Recalls & reported problems
Becton, Dickinson And Company · BD Multi-Check™ CD4 Low Control · 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
- Oct 5, 2020Terminated
Recent product complaints showing an unexpected cell population exhibiting dim CD3 expression that may result in inaccurate results gating.
Z-0562-2021 · Root cause: Process control · FDA record ↗
Other Mixture, hematology quality control devices
- BD Multi-Check 349703Becton, Dickinson And Company · Mixture, hematology quality control1 recall1 report
- BD Multi-Check 349704Becton, Dickinson And Company · Mixture, hematology quality control1 recall1 report
- Research and Diagnostic Systems D3D04Research And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 reports
- Research and Diagnostic Systems D3D02Research And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 reports
- Research and Diagnostic Systems 3D503RXResearch And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 reports
- BD Trucount 340335Becton, Dickinson And Company · Mixture, hematology quality control1 recall0 reports
- Research and Diagnostic Systems 3D506USResearch And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 reports
- Research and Diagnostic Systems 3D503Research And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 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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