Hunstad Infiltration Handle HUN-HANRecalls & reported problems
Mentor Texas L.P. · Hunstad Infiltration Handle · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00081317023173), received between Mar 18, 2025 and Mar 18, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (3 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 18, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT A HUNSTAD INFILTRATION HANDLE LEAKED DURING A ABDOMINOPLASTY SURGERY. HOWEVER, THE SURGERY WAS COMPLETED WITH THE HANDLE AND WITHOUT ANY REPORTED DELAYS. NO ADVERSE EVENTS OR PATIENT CONSEQUENCES WERE REPORTED. SEVERAL FOLLOW-UPS HAVE BEEN CONDUCTED, AND NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. IF MORE INFORMATION BECOMES AVAILABLE, MENTOR WILL SUBMIT A SUPPLEMENTAL REPORT ACCORDINGLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21634984 ↗MalfunctionMar 18, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT A HUNSTAD INFILTRATION HANDLE LEAKED DURING A ABDOMINOPLASTY SURGERY. HOWEVER, THE SURGERY WAS COMPLETED WITH THE HANDLE AND WITHOUT ANY REPORTED DELAYS. NO ADVERSE EVENTS OR PATIENT CONSEQUENCES WERE REPORTED. SEVERAL FOLLOW-UPS HAVE BEEN CONDUCTED, AND NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. IF MORE INFORMATION BECOMES AVAILABLE, MENTOR WILL SUBMIT A SUPPLEMENTAL REPORT ACCORDINGLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21634983 ↗MalfunctionMar 18, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT A HUNSTAD INFILTRATION HANDLE LEAKED DURING A ABDOMINOPLASTY SURGERY. HOWEVER, THE SURGERY WAS COMPLETED WITH THE HANDLE AND WITHOUT ANY REPORTED DELAYS. NO ADVERSE EVENTS OR PATIENT CONSEQUENCES WERE REPORTED. SEVERAL FOLLOW-UPS HAVE BEEN CONDUCTED, AND NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. IF MORE INFORMATION BECOMES AVAILABLE, MENTOR WILL SUBMIT A SUPPLEMENTAL REPORT ACCORDINGLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21634981 ↗
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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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