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Formula 0375627000Recalls & reported problems

Stryker Corporation · [Small-Joint Full Radius Cutter, Arthroscopic Shaver Blade, Do Not Resterilize, Do Not Use if Package is Damaged, Keep Dry, Keep Away from Sunlight] · 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 07613327061949), received between Oct 22, 2018 and Oct 22, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Thermal Decomposition of 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

  • Thermal Decomposition of Device1

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.

  • MalfunctionOct 22, 2018Thermal Decomposition of Device

    IT WAS REPORTED THAT THE BASE PLASTIC COMPONENT WAS BURNED BY THE HEAT OF THE FRICTION AT THE BUR SHAFT AND THERE WERE NO BURNS TO THE PATIENT OR USERS.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7991487 ↗

Other BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL devices

All BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL devices →

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