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Formula 0375832000Recalls & reported problems

Stryker Corporation · Subchondral Drill, 1.5 mm Drill Tip. Arthroscopic Shaver Blade. For use with: REF 0375-701-500, 0375-704-500, 0375-708-500. Do Not Use if Package is Damaged, Keep Dry, Keep Away from Sunlight · Class 1

All models of Formula (43)

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 07613327062052), received between Oct 11, 2022 and Oct 11, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1
  • Retraction Problem1

Patient problems

  • Foreign Body In Patient1
  • 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.

  • MalfunctionOct 11, 2022Retraction Problem; Detachment of Device or Device Component; Retraction Problem

    IT WAS REPORTED THAT THE TIP OF THE DRILL REMAINED IN THE PATIENT WHICH REQUIRED A REVISION SURGERY TO REMOVE.

    Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions

    MAUDE report 15575801 ↗

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

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Sources and updates

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