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Crossblade 0485840000Recalls & reported problems

Stryker Corporation · XL, Arthroscopic Shaver Blades, Diamond Round Bur. 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 07613327301533), received between Apr 26, 2022 and Apr 26, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (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

  • Material Deformation1
  • Melted1
  • Overheating of Device1

Patient problems

  • Insufficient Information1
  • 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.

  • MalfunctionApr 26, 2022Melted; Overheating of Device; Material Deformation; Material Deformation

    IT WAS REPORTED THAT THE DEVICE OVERHEATED AND MELTED THE PLASTIC ON THE DEVICE.

    Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

    MAUDE report 14215172 ↗

Other BUR, SURGICAL, GENERAL & PLASTIC SURGERY devices

All BUR, SURGICAL, GENERAL & PLASTIC SURGERY devices →

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