MEDLINE SLIDEBR25GRecalls & reported problems
Medline Industries, Inc. · SLIDE BLOOD COLLECTION SET, 25GX0.75 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10197344098798), received between Sep 12, 2026 and Sep 17, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Material Too Soft/Flexible1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Detachment of Device or Device Component
The report states, "After receiving a flash with the butterfly needle, I attached the needed blood tube to the needle holder and held both firmly as the blood tubes will pop off. The needle holder and the blood tube stayed safely in one hand, (the other hand was still holding the butterfly wings of the needle in the patient's arm), but the tube plug puncture needle in the needle seat popped out of the needle holder. The plug puncture needle is covered in a rubber sleeve that prevented contact with that needle. I thought it was user error and that I did not screw the needle holder on tightly and reattached the needle holder as tightly as I could. When I inserted the blood tube, it happened again and I quit that blood draw."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50804956 ↗MalfunctionSep 12, 2026Material Too Soft/Flexible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746507 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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