REFLECTION, MICROSTABLE 71742846Recalls & reported problems
Smith & Nephew, Inc. · REFLECTION LINER 28 INNER DIAMETER 46-48 OUTER DIAMETER 20 DEGREE SIZE D · Class 2
All models of REFLECTION, MICROSTABLE (16)
Data updated Oct 16, 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 03596010232250), received between Jun 1, 2017 and Sep 28, 2021 — classified as 2 injuries.
The most frequently reported specific device problem is “Naturally Worn” (2 reports).
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
Device problems
- Naturally Worn2
- Degraded1
Patient problems
- Failure of Implant1
- Insufficient Information1
- No Code Available1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 28, 2021Naturally Worn; Naturally Worn
IT WAS REPORTED THAT, AFTER THR SURGERY HAD BEEN PERFORMED ON 2004, AN EXETER STEM BROKE. A REVISION SURGERY WAS PERFORMED ON (B)(6) 2021. DURING THIS SURGERY, THE REF LNR 28ID 20 DEG SZ D WAS EXCHANGED. CURRENT HEALTH STATUS OF PATIENT IS UNKNOWN. THE REASON FOR CHANGING THE LINER WAS BECAUSE THE DEVICE WAS WORN.
Patient problems: Insufficient Information
MAUDE report 12543470 ↗InjuryJun 1, 2017Degraded; Naturally Worn; Degraded
IT WAS REPORTED THAT PATIENT UNDERWENT A REVISION SURGERY WITH REPLACEMENT OF LINER DUE TO SIGNIFICANT WEAR. SAME SIZE LINER WAS IMPLANTED.
Patient problems: Failure of Implant; No Code Available
MAUDE report 6603954 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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