LAMIS 14ga x 23cm Infiltration Cannula BN1423Recalls & reported problems
Mentor Texas L.P. · LAMIS 14ga x 23cm Infiltration Cannula · 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 00081317022534), received between Feb 25, 2019 and Feb 25, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Connection Problem” (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.
Most reported problems
Device problems
- Connection Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 25, 2019Connection Problem; Connection Problem
IT WAS REPORTED THAT PRIOR TO A UNSPECIFIED SURGERY WHEN A FACILITY REPLACED A HANDLE FROM A LAMIS 14GA X 23CM INFILTRATION CANNULA, THINKING IT WAS THE HANDLE, THE CANNULA STARTED LEAKING MORE. THERE WAS NO PATIENT CONSEQUENCE REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8367890 ↗
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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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