Maveric Medical M6234Recalls & reported problems
Maveric Medical LLC · Blood Collection Set, Safety, 23G x 3/4", 12" Tubing, Luer Adapter · Class 2
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 00850028131046), received between Apr 14, 2026 and Apr 14, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fail-Safe Did Not Operate” (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
- Fail-Safe Did Not Operate1
- 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.
MalfunctionApr 14, 2026Fail-Safe Did Not Operate; Lack of Effect
COMPLAINT 1: PHLEBOTOMIST EXPERIENCED ISSUE THIS MORNING WHEN USING THE HOSPITAL'S NEW MAVERIC BUTTERFLY. THE TUBING PROTRUDED FROM THE SIDE OF THE SAFETY SLEEVE AND PREVENTED PROPER ACTIVATION OF THE SAFETY DEVICE. THE PHLEBOTOMIST STATES THIS IS THE SECOND TIME THIS HAS HAPPENED. SEE SAMPLE PHOTO BELOW OF REPORTED ISSUE: COMPLAINT 2: THE ASSOCIATES INCLUDING OUR LEAD PHLEBOTOMIST SHARED THAT THE NEW BUTTERFLY DEVICES ARE DIFFICULT TO USE. THEY ARE HARD TO MANEUVER. THEY DON'T SEE THE FLASH. EVEN THOUGH YOU'RE IN THE VEIN, THE BLOOD FLOW IS SLUGGISH. AS STATED, ENGAGING THE SAFETY IS DIFFICULT. THEY HAVE CONCERNS THAT A POTENTIAL SHARPS INJURY WILL LIKELY OCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24870249 ↗
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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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