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RADIUS 486611640Recalls & reported problems

Stryker Corporation · MULTI-ANGLE SCREW · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540544483), received between Apr 29, 2019 and Apr 29, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Device Slipped” (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

  • Device Slipped1
  • Migration1

Patient problems

  • Discomfort1
  • Injury1
  • Pain1

Recent adverse event reports

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

  • InjuryApr 29, 2019Device Slipped; Migration; Migration

    THE DEVICE WAS IMPLANTED (B)(6) 2016. THE PATIENT BEGAN TO EXPERIENCE DISCOMFORT ATTRIBUTED TO THE CONCOMITANTLY IMPLANTED CAGE IN (B)(6) 2017. REVISION SURGERY WAS PERFORMED TO ADDRESS THE CONCOMITANT DEVICE ON (B)(6) 2019. DURING REVISION, THE PHYSICIAN NOTED THAT THIS DEVICE (L4 SCREW) WAS, "SLIGHTLY LOOSE," THEN REMOVED AND REPLACED IT.

    Patient problems: Discomfort; Injury; Pain

    MAUDE report 8563273 ↗

Other APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices

All APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices →

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