LAMIS 14ga x 30cm Infiltration Cannula BN1430Recalls & reported problems
Mentor Texas L.P. · LAMIS 14ga x 30cm Infiltration Cannula · Class 2
Data updated Oct 18, 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 00081317022541), received between Aug 29, 2020 and Sep 8, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 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.
Most reported problems
Device problems
- Fluid/Blood Leak2
- Fracture1
Patient problems
- No Patient Involvement2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2020Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT A LAMIS 14GA X 30CM INFILTRATION CANNULA WAS FOUND TO BE LEAKING NEAR THE HUB PREOPERATIVELY. THERE WAS NO PATIENT CONTACT WITH THE DEVICE, NOR ANY REPORTED PROCEDURAL DELAYS.
Patient problems: No Patient Involvement
MAUDE report 10505112 ↗MalfunctionAug 29, 2020Fluid/Blood Leak; Fracture; Fluid/Blood Leak; Fracture
IT WAS REPORTED THAT A LAMIS 14GA X 30CM INFILTRATION CANNULA WAS BROKEN AT THE HUB AND DEVELOPED A LEAK PRE-OPERATIVELY. THERE WAS NO PATIENT INVOLVEMENT, NO ADVERSE EVENT REPORTED.
Patient problems: No Patient Involvement
MAUDE report 10469606 ↗
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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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