Prime P3CIMPADRecalls & reported problems
Microport Orthopedics Inc. · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684P3CIMPAD1), received between Oct 28, 2021 and Oct 28, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Residue After Decontamination” (2 reports).
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
- Residue After Decontamination2
- Device Dislodged or Dislocated1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 28, 2021Residue After Decontamination; Residue After Decontamination
ALLEGEDLY, DEVICES HAD BLOOD WASTE FROM PREVIOUS OPERATIONS.
Patient problems: Insufficient Information
MAUDE report 12716537 ↗MalfunctionOct 28, 2021Residue After Decontamination; Device Dislodged or Dislocated; Residue After Decontamination; Device Dislodged or Dislocated
ALLEGEDLY, DEVICES HAD BLOOD WASTE FROM PREVIOUS OPERATIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12713900 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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