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3M™ 9690 (UDI 50707387575217)Recalls & reported problems

3m Company · 3M™ Single-Use Specialty Clipper Blade Assembly 9690 · Class 1

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 50707387575217), received between Feb 12, 2019 and Feb 12, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Defective Device” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Defective Device1

Patient problems

  • Abrasion2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 12, 2019Defective Device

    DURING PATIENT PREP, THE CLIPPER CAUSED SMALL CUT/ABRASION TO AREA BEING TRIMMED. THE AREA WAS CLEANSED PER MEDICAL DOCTOR ORDER. NO FURTHER INTERVENTION REQUIRED.

    Patient problems: Abrasion

    MAUDE report 8330682 ↗
  • MalfunctionFeb 12, 2019Adverse Event Without Identified Device or Use Problem

    DURING PRE-OP PREP OF PATIENT, CLIPPERS USED AND ABRASION TO SKIN NOTED AT SITE AFTER USE. MD AWARE, SITE CLEANSED, NO FURTHER INTERVENTION REQUIRED.

    Patient problems: Abrasion

    MAUDE report 8330675 ↗

Other RAZOR, SURGICAL devices

All RAZOR, SURGICAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.