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R3 ACETABULAR 71338948Recalls & reported problems

Smith & Nephew, Inc. · R3 32MM ID US CERAMIC ACET LINER MM48 · Class 3 · Implant

All models of R3 ACETABULAR (24)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556022047), received between Feb 10, 2018 and Jun 25, 2018 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (1 report).

6 other recalls cover devices cleared under the same FDA submission (P030022); 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

Device problems

  • Break1
  • Fracture1

Patient problems

  • Injury2

Recent adverse event reports

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

  • InjuryJun 25, 2018Break; Break

    IT WAS REPORTED THAT A PATIENT CAME INTO THE CLINIC COMPLAINING THAT SHE HEARD A CRACK OR POP WHILE WALKING. DOCTOR INFORMED THAT THE R3 CERAMIC LINER IS BROKEN.

    Patient problems: Injury

    MAUDE report 7632976 ↗
  • InjuryFeb 10, 2018Fracture; Fracture

    IT WAS REPORTED THAT SURGEON REVISED R3 CERAMIC LINER DUE TO FAILURE. LINER HAD FRACTURED IN MULTIPLE POINTS IN LOAD BEARING REGION. AFTER PIECES WERE REMOVED, A NEW PLASTIC LINER WAS PLACED IN THE EXISTING CUP.

    Patient problems: Injury

    MAUDE report 7262508 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P030022. One submission often covers many models, so check the product and lot details in each record.

  • Z-2056-2011 · Mar 11, 2011 · Terminated
    R3 TM CERAMIC ACETABULAR LINER, BIOLOX FORTE, 36 MM O.D. 54 MM O.D., REF 71338954, STERILE R, QTY (1), Smith & Nephew, Inc., Memphis, TN 38116, 2017/06
  • Z-2057-2011 · Mar 11, 2011 · Terminated
    R3 TM CERAMIC ACETABULAR LINER, BIOLOX FORTE, 36 MM O.D. 56 MM O.D., REF 71338956, STERILE R, QTY (1), Smith & Nephew, Inc., Memphis, TN 38116, 2017/06
  • Z-2055-2011 · Mar 11, 2011 · Terminated
    R3 TM CERAMIC ACETABULAR LINER, BIOLOX FORTE, 36 MM O.D. 52 MM O.D., REF 71338952, STERILE R, QTY (1), Smith & Nephew, Inc., Memphis, TN 38116, 2017/06
  • Z-2058-2011 · Mar 11, 2011 · Terminated
    R3 TM CERAMIC ACETABULAR LINER, BIOLOX FORTE, 36 MM O.D. 62 MM O.D., REF 71338962, STERILE R, QTY (1), Smith & Nephew, Inc., Memphis, TN 38116, 2017/06
  • Z-2053-2011 · Mar 11, 2011 · Terminated
    R3 TM CERAMIC ACETABULAR LINER, BIOLOX FORTE, 32 MM I.D. 48 MM O.D., REF 71338948, STERILE R, QTY (1), Smith & Nephew, Inc., Memphis, TN 38116, 2017/06 Usage: Primary total
  • Z-2054-2011 · Mar 11, 2011 · Terminated
    R3 TM CERAMIC ACETABULAR LINER, BIOLOX FORTE, 32 MM O.D. 55 MM O.D., REF 71338950, STERILE R, QTY (1), Smith & Nephew, Inc., Memphis, TN 38116, 2017/06

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices

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Sources and updates

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