BD Seditainer™ 0.105M 1.25ml Buffered Sodium Citrate Blood Collection Tubes 366065Recalls & reported problems
Becton, Dickinson U.K. Limited · BD Seditainer™ Buff.Na Citrate 0.105M 1.25ml · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 30382903660651), received between May 8, 2018 and Aug 22, 2019 — classified as 4 malfunctions.
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 18, 2026.
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings1
- Leak/Splash1
- Overfill1
- Short Fill1
Patient problems
- No Known Impact Or Consequence To Patient3
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 22, 2019Leak/Splash; Leak/Splash
IT WAS REPORTED THAT DURING R&D TESTING AT BD, A GLASS TUBE WAS FOUND TO BE BROKEN UPON RECEIPT WITH A BD SEDITAINER¿ 0.105M 1.25ML BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: DURING R&D TESTING IN, WE OBSERVED A GLASS TUBE THAT WAS RECEIVED AS CRACKED/BROKEN AT THE TUBE TOP (UNDERNEATH THE HEMOGARD¿ CLOSURE).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8921643 ↗MalfunctionJan 25, 2019Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WITH THE USE OF THE BD SEDITAINER¿ 0.105M 1.25ML BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBES THERE WAS AN ISSUE WITH AFTER CENTRIFUGATION THE SAMPLE WAS CLOTTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8277892 ↗MalfunctionNov 12, 2018Overfill; Overfill
IT WAS REPORTED WITH THE USE OF THE BD SEDITAINER¿ 0.105M 1.25ML BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBES THERE WAS AN ISSUE WITH OVERFILL. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8059756 ↗MalfunctionMay 8, 2018Short Fill; Short Fill
IT WAS REPORTED THAT BD SEDITAINER¿ 0.105M 1.25ML BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBES HAD ISSUES WITH UNDERFILL.
Patient problems: No Information
MAUDE report 7494944 ↗
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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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