Skip to content

Arthrex® AR-523-A214Recalls & reported problems

Arthrex, Inc. · CR Plus Tibial Bearing, Sz 2, 14mm · Class 2 · Implant

Data updated Oct 18, 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 00888867231214), received between Jun 14, 2018 and Jun 14, 2018 — classified as 1 injury.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Lupus1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJun 14, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT UNDERWENT A TOTAL KNEE REPLACEMENT ON (B)(6) 2018 WHERE A SIZE 2 CR PLUS TIBIAL BEARING, AR-523-A214, WAS IMPLANTED. THE PATIENT CONTRACTED AN INFECTION IN THE KNEE AND ON (B)(6) 2018, A LINEAR EXCHANGE WAS PERFORMED AND THE TIBIAL BEARING WAS EXPLANTED. THE PATIENT HAS LUPUS AND IS BEING TREATED WITH ANTIBIOTICS. THE EXPLANTED BEARING HAS BEEN SENT TO PATHOLOGY FOR FURTHER TESTING. PATIENT IS A FEMALE, (B)(6).

    Patient problems: Lupus; Unspecified Infection

    MAUDE report 7600200 ↗

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page