BD Vacutainer® CTAD 367947Recalls & reported problems
Becton, Dickinson U.K. Limited · BD Vacutainer® CTAD · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 50382903679473), received between May 11, 2018 and Sep 17, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Incorrect Or Inadequate Test Results” (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 18, 2026.
Most reported problems
Device problems
- Incorrect Or Inadequate Test Results1
- Overfill1
- Short Fill1
Patient problems
- No Information2
- No Patient Involvement1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2020Overfill; Overfill
IT WAS REPORTED DURING USE THE BD VACUTAINER® CTAD (BUFFERED SODIUM CITRATE THEOPHYLLINE ADENOSINE DIPYRIDAMOLE) BLOOD COLLECTION TUBES EXPERIENCED OVERFILL. THIS EVENT OCCURRED 2 TIMES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE CUSTOMER STATED THE TUBES "ARE FILLING ALL THE WAY TO THE TOP PASSING THE LINE REQUIRED FOR BLOOD DRAW.¿
Patient problems: No Patient Involvement
MAUDE report 10549347 ↗MalfunctionMay 29, 2018Incorrect Or Inadequate Test Results; Incorrect Or Inadequate Test Results
IT WAS REPORTED THAT BD VACUTAINER® CTAD BLOOD COLLECTION TUBES HAD "INCORRECT OR INADEQUATE TEST RESULTS".
Patient problems: No Information
MAUDE report 7548939 ↗MalfunctionMay 11, 2018Short Fill; Short Fill
IT WAS REPORTED THAT BD VACUTAINER® CTAD BLOOD COLLECTION TUBES HAD "UNDERFILL"
Patient problems: No Information
MAUDE report 7506938 ↗
Other Tubes, vials, systems, serum separators, blood collection devices
- BD Vacutainer® SST™ 367986Becton, Dickinson And Company · Tubes, vials, systems, serum separators, blood collection2 recalls2,711 reports
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- BD Vacutainer® SST™ II Advance 367955Becton, Dickinson U.K. Limited · Tubes, vials, systems, serum separators, blood collection1,478 reports
- BD Vacutainer® Eclipse™ Blood Collection Needle 368607Becton, Dickinson And Company · Tubes, vials, systems, serum separators, blood collection1,220 reports
- BD Vacutainer® SST™ 367983Becton, Dickinson And Company · Tubes, vials, systems, serum separators, blood collection2 recalls1,075 reports
- BD Vacutainer® K2 EDTA (K2E) 5.4mg Blood Collection Tubes 367856Becton, Dickinson And Company · Tubes, vials, systems, serum separators, blood collection1,010 reports
- BD Vacutainer® PST™ Gel and Lithium HeparinN 56 Units 367960Becton, Dickinson And Company · Tubes, vials, systems, serum separators, blood collection1 recall747 reports
- BD Vacutainer® SST™ II Advance 367957Becton, Dickinson U.K. Limited · Tubes, vials, systems, serum separators, blood collection767 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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