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RHEAD 310-0010Recalls & reported problems

Stryker GmbH · Lateral Assembly, Radial Stem Head Implant, Size 4 · Class 2 · Implant

All models of RHEAD (12)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00886385022772), received between Dec 13, 2018 and Dec 13, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1

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.

  • InjuryDec 13, 2018Device Dislodged or Dislocated

    PATIENT WAS LIFTING A BOX OVERHEAD, LATERAL RADIAL HEAD DISLODGED FROM STEM. BOTH HEAD AND STEM IMPLANTS WERE EXPLANTED. COMPETITIVE PRODUCT USED AS REPLACEMENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8162202 ↗

Other PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER devices

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Sources and updates

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