Medline DYNDSBCHLDRRecalls & reported problems
Medline Industries, Inc. · SAFETY TUBE HOLDER, BLOOD COLLECTION · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 20193489008422), received between Sep 24, 2022 and Sep 11, 2026 — classified as 2 injuries, 5 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (4 reports).
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
- Material Twisted/Bent4
- Appropriate Device Problem Term/Code Not Available1
- Device Fell1
- Material Puncture/Hole1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Exposure to Body Fluids2
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 11, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50736032 ↗MalfunctionSep 11, 2026Material Twisted/Bent
It was reported that "The needle bent trying to engage the safety and the Safety will not stay engaged."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50731903 ↗MalfunctionSep 10, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50718509 ↗MalfunctionSep 9, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701717 ↗MalfunctionSep 9, 2026Material Puncture/Hole
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50697528 ↗InjuryJan 18, 2023Device Fell; Device Fell
ACCORDING TO THE CUSTOMER, ON (B)(6) 2022 'WHILE THE NURSE TRIED TO PUT THE SAFETY CAP ON, IT BROKE OFF THE TOP OF THE LUER, AND BLOOD SPRAYED ALL OVER THE NURSE'S FACE AND IN HER LEFT EYE'.
Patient problems: Exposure to Body Fluids
MAUDE report 16195364 ↗InjurySep 24, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2022 'THE BUTTERFLY NEEDLE WAS REMOVED FROM THE PATIENTS ARM AND PULLED UP TO PUT THE SAFETY LOCK ON THE NEEDLE, AND ONCE THEY PULLED UP THE LINE DETACHED FROM THE HUB SPLASHING BLOOD EVERYWHERE'. PER THE FACILITY THE EMPLOYEE WAS PUT ON A 5 DAY MEDICATION CALLED PREP AND WAS REQUIRED TO HAVE BLOOD WORK DONE, WITH ADDITIONAL BLOOD WORK REQUIRED IN 6 MONTHS.
Patient problems: Exposure to Body Fluids
MAUDE report 15477108 ↗
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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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