REDAPT 71354802Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556579916), received between Sep 22, 2021 and Sep 22, 2021 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K162303, K211176); 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 16, 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.

• InjurySep 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT, 6 WEEKS AFTER A MEDICALLY INDICATED REVISION OF THE LEFT HIP THA PERFORMED ON (B)(6) 2018 TO TREAT TROCHANTERIC FEMORAL FRACTURES, WHERE REDAPT SLVD MONO STEM 240MM SZ 13 SO WAS IMPLANTED, THE PATIENT REQUIRED A SECOND REVISION SURGERY DUE TO A LEFT VANCOUVER B2 PERIPROSTHETIC FEMUR FRACTURE. THERE IS ALSO A REPORT FOR AN ADVERSE EVENT, OCCURRED ON (B)(6) 2018, FOR A RUPTURE OF THE MOST INFERIOR CABLE ATTACHED TO A FEMORAL PLATE, ALTHOUGH IT IS UNKNOWN IF THESE DEVICES ARE SMITH AND NEPHEW DEVICES. ADDITIONAL DETAILS ABOUT PRIMARY SURGERY AND THE PATIENT'S FINAL OUTCOME ARE UNKNOWN. THIS DE-IDENTIFIED CLINICAL DATA IS RELATED TO A POST MARKET CLINICAL FOLLOW-UP ACTIVITY FOR REDAPT SLEEVED MONO STEMS. AS THE DATA COLLECTION ACTIVITY HAS BEEN DONE RETROSPECTIVELY AND DATA IS PROVIDED ANONYMIZED, THE INFORMATION PROVIDED IS LIMITED AND FURTHER INFORMATION CANNOT BE OBTAINED.

  Patient problems: Bone Fracture(s); Failure of Implant; Vertebral Fracture

  MAUDE report 12513808 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K162303, K211176. One submission often covers many models, so check the product and lot details in each record.

• Z-0326-2025 · Oct 15, 2024 · Open, Classified
  Tandem Intl Bipolar Cocr Shell/UHMWPE Liner, TI-6AL-4V Retaining Ring, 28MM I.D. 46 MM O.D., REF 71324046, sterile, femoral head bipolar component of the Tandem Bipolar Hip System.