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V. Mueller SU3660Recalls & reported problems

Steris Corporation · V. Mueller USA RETRACTOR DOUBLE-ENDED SET OF 2 OVERALL LENGTH 8 inches 20.3CM · Class 1

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 10885403132803), received between Mar 8, 2022 and Mar 8, 2022 — classified as 1 malfunction.

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

  • Crack1
  • Excessive Heating1
  • Fail-Safe Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMar 8, 2022Crack; Fail-Safe Problem; Excessive Heating; Excessive Heating

    IT WAS REPORTED THAT THERE WAS A BURN ON PATIENT'S SKIN WHEN INSULATED ARMY NAVY RETRACTOR WAS MOVED. OPERATOR NOTICED CRACKS IN THE INSULATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13694758 ↗

Other RETRACTOR devices

All RETRACTOR devices →

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