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REDAPT 71354713Recalls & reported problems

Smith & Nephew, Inc. · REDAPT 240MM SLEEVELESS REVISION STEM SIZE 23 STANDARD OFFSET · Class 2 · Implant

Data updated Oct 13, 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 00885556579374), received between Nov 12, 2019 and Nov 12, 2019 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (K151902, 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Injury1

Recent adverse event reports

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

  • InjuryNov 12, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT SURGEON WAS PERFORMING A REVISION HIP, REMOVING A BHR CUP AND EMPERION STEM WITH BHR MODULAR HEAD. HE REPLACED THIS WITH A 76 MM R3 MUTLIHOLE SHELL, A 40 MM ZERO DEGREE LINER AND A 23 MM X 240 MM SLEEVELESS REDAPT STEM. DURING THE TRIALLING STAGE IT WAS FOUND THAT THE SHOULDER OF THE STEM IMPINGED ON THE RIM OF THE CUP AT AROUND THE 10 O CLOCK POSITION DURING ABDUCTION AND EXTERNAL ROTATION OF THE LIMB. HE TRIED VARIOUS COMBINATIONS OF HEAD LENGTHS, OFFSET LINER AND NECK OPTIONS. HE FEELS THE CUP VERSION IS NORMAL AND THE SHOULDER OF THE STEM SHOULD NOT IMPINGE AT THIS POINT. NO MORE INFORMATION AVAILABLE.

    Patient problems: Injury

    MAUDE report 9310022 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K151902, 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.

Other Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate devices

All Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate devices →

Sources and updates

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