BD Multi-Check 349701Recalls & reported problems
Becton, Dickinson And Company · BD Multi-Check™ Control · Class 2
All models of BD Multi-Check (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382903497010), received between Jul 20, 2023 and Jul 20, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (1 report).
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 16, 2026.
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 20, 2023Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT DURING USE WITH THE BD MULTI-CHECK CONTROL THERE WAS INCORRECT LABEL INFORMATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE THE INITIAL REPORTER: IT WAS REPORTED BY THE CUSTOMER THAT WHEN THE R&D MULTI-CHECK CONTROLS (349701 AND 349704) COME DIRECTLY FROM R&D, THE 2D BARCODE CAN BE READ BY THE FACSDUET. BUT WHEN THE R&D CONTROLS ARE REPACKAGED FOR BDB THE QR BARCODE ON THE TUBE IS NOT COMPATIBLE WITH THE DUET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17359069 ↗
Other Mixture, hematology quality control devices
- BD Multi-Check 349704Becton, Dickinson And Company · Mixture, hematology quality control1 recall1 report
- BD Multi-Check 349703Becton, 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 3D503RXResearch And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 reports
- Research and Diagnostic Systems 3D501Research And Diagnostic Systems, Inc. · Mixture, Hematology Quality Control1 recall0 reports
- Research and Diagnostic Systems 3D507Research And Diagnostic Systems, Inc. · 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 D3D02Research 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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