Duracon 6742-1-311Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540324030), received between Dec 16, 2019 and Dec 16, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K012172); they may or may not involve this specific model.

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

• InjuryDec 16, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  AS REPORTED: "JOINT LAXITY RIGHT TOTAL KNEE. DID POLY SWAP." A 3X11 DURACON PS INSERT WAS REVISED.

  Patient problems: Injury

  MAUDE report 9476459 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K012172. One submission often covers many models, so check the product and lot details in each record.

• Z-0924-2024 · Dec 1, 2023 · Open, Classified
  PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413
• Z-0923-2024 · Dec 1, 2023 · Open, Classified
  PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411