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MicroAire® PAL-R408LLRecalls & reported problems

Microaire Surgical Instruments LLC · 4mm MULTI-USE CANNULA, 10mm PORT, 30cm LONG, FLARED MERCEDES · 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 00847399009234), received between Mar 6, 2020 and Mar 6, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 6, 2020Break

    CUSTOMER HAS REPORTED THAT DURING A LIPOSUCTION PROCEDURE, THE TIP OF THE LIPOSUCTION CANNULA BROKE OFF IN THE PATIENT'S SUB-CUTANEOUS TISSUE. IT WAS NECESSARY FOR THE PATIENT TO RECEIVE AN X-RAY AND FOR THE TIP TO BE EXTRACTED. THIS EXTENDED THE PROCEDURE BY APPROXIMATELY ONE (1) HOUR. THERE WAS NO PATIENT INJURY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9802781 ↗

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Sources and updates

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