Implant Partners EAI3110LWDRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684EAI3110LWD1), received between Mar 16, 2020 and Mar 16, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 16, 2020Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

  ALLEGEDLY, THE PATIENT WAS IMPLANTED WITH THE EVOLUTION NITRIX (TIBIAL AND FEMORAL COMPONENTS) BUT SURGERY WAS COMPLETED WITHOUT A TIBIA INSERT BECAUSE THE HOSPITAL ONLY HAD IMPLANT PARTNER INSERTS AVAILABLE WHICH ARE NOT INDICATED FOR USE WITH THE EVOLUTION NITRIX. THE INSERT WAS LATER IMPLANTED WHICH WOULD WORK WITH THE TIBIAL AND FEMORAL COMPONENTS. THERE WAS A SECONDARY SURGERY DUE TO A NON-COMPATIBLE INSERT FOR THE ORIGINAL SURGERY.

  Patient problems: No Information

  MAUDE report 9835696 ↗
• InjuryMar 16, 2020Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

  ALLEGEDLY, THE PATIENT WAS IMPLANTED WITH THE EVOLUTION NITRIX (TIBIAL AND FEMORAL COMPONENTS) BUT SURGERY WAS COMPLETED WITHOUT A TIBIA INSERT BECAUSE THE HOSPITAL ONLY HAD IMPLANT PARTNER INSERTS AVAILABLE WHICH ARE NOT INDICATED FOR USE WITH THE EVOLUTION NITRIX. THE INSERT WAS LATER IMPLANTED WHICH WOULD WORK WITH THE TIBIAL AND FEMORAL COMPONENTS. THERE WAS A SECONDARY SURGERY DUE TO A NON-COMPATIBLE INSERT FOR THE ORIGINAL SURGERY.

  Patient problems: No Information

  MAUDE report 9835639 ↗