PROFEMUR® PPW39110Recalls & reported problems
Microport Orthopedics Inc. · "PROFEMUR® R" GRIT BLASTED PROX BODY STD 4 V4 · 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 M684PPW391101), received between Mar 5, 2025 and Mar 5, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 5, 2025Break; Break
ALLEGEDLY, BREAKAGE OF THE PART AND REVISION SURGERY DONE AS A CONSEQUENCE.
Patient problems: Insufficient Information
MAUDE report 21532245 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.