CARDINAL HEALTH BTA200Recalls & reported problems
Cardinal Health 200, LLC · Blood Transfer Adapter · Class 1
Data updated Oct 18, 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 10885380182952), received between Dec 13, 2025 and Dec 13, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Lack of Effect” (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.
Reports received per month
Most reported problems
Device problems
- Lack of Effect1
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.
MalfunctionDec 13, 2025Lack of Effect; Lack of Effect
BLOOD SPECIMENS COULD NOT BE TRANSFERRED INTO BLOOD CULTURE BOTTLES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23797155 ↗
Other System, Blood Collection, Vacuum-Assisted, Manual devices
- IV Plus® BD6010Nexus Medical, LLC · System, Blood Collection, Vacuum-Assisted, Manual6 reports
- Multi-Sampling Connector 4R5129Fresenius Kabi AG · System, Blood Collection, Vacuum-Assisted, Manual2 reports
- CARDINAL HEALTH BCA200Cardinal Health 200, LLC · System, blood collection, vacuum-assisted, manual2 reports
- MediChoice BTD002Owens & Minor Distribution, Inc. · System, blood collection, vacuum-assisted, manual1 report
- MEDLINE DYNDBCHLDRMedline Industries, Inc. · System, blood collection, vacuum-assisted, manual1 report
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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