MediChoice BTD002Recalls & reported problems
Owens & Minor Distribution, Inc. · Device Blood Transfer With Female Connector For Use With Luer Syringes Not Made With Natural Rubber Latex Transparent Blue MediChoice · Class 1
- 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 10885632136764), received between Nov 24, 2023 and Nov 24, 2023.
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.
Reports received per month
Most reported problems
Patient problems
- Exposure to Body Fluids1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
OtherNov 24, 2023
HAD 3 KNOWN INSTANCES WHERE THE BLACK NEEDLE PIECE IN THE BLOOD TRANSFER DEVICE BECAME DETACHED FROM THE REST OF THE BLOOD TRANSFER DEVICE. ONE WAS SUCKED INTO A BLOOD CULTURE BOTTLE. THE OTHER TWO WERE ABLE TO BE REMOVED FROM THE BOTTLES. HOWEVER, THESE PUT PATIENTS AND PERSONNEL AT RISK TO INFECTIOUS MATERIAL, BLOOD BORNE PATHOGENS AND UNNECESSARY TREATMENT. ONE OF THE PHLEBOTOMISTS WAS SPRAYED BY BLOOD DUE TO THE FAILURE. REFERENCE REPORT #MW5148488, #MW5148489.
Patient problems: Exposure to Body Fluids
MAUDE report 18208902 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.