NA 1011-72-000Recalls & reported problems
Depuy Orthopaedics, Inc. · PROTRUSIO CAGE CEMENTED ACETABULAR RECONSTRUCTION 52mm OD 49mm ID LEFT · Class 2 · Implant
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 10603295000549), received between Mar 8, 2021 and Jun 17, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (1 report).
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
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
Patient problems
- Adhesion(s)1
- Insufficient Information1
- Scar Tissue1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 17, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PC WAS CREATED TO CAPTURE THE EVENT. (PG 2560) ON (B)(6) 2009 OPERATIVE RECORDS INDICATE THE PATIENT RECEIVED A LEFT TOTAL HIP REVISION DUE TO SIGNIFICANT SCARRING AND GROSS INFECTION. ACETABULAR CAGE AND PROSTALAC WAS REMOVED AND IRRIGATION AND DEBRIDEMENT WAS PERFORMED. DOI: (B)(6) 2009. DOR: (B)(6) 2009. LEFT HIP.
Patient problems: Adhesion(s); Scar Tissue; Unspecified Infection
MAUDE report 14732251 ↗InjuryMar 8, 2021Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT BROKE THE PROTRUSIO CAGE AND A FEW SCREWS IMPLANTED BACK IN 2019. SURGEON REMOVED ALL CAGE AND SCREWS ALONG WITH A CEMENTED CUP AND REPLACED WITH A PINNACLE REVISION CUP AND USED DUAL MOBILITY TO HELP PATIENT WITH STABILITY. NO SURGICAL DELAY. DOI: (B)(6) 2019, DOR: (B)(6) 2021, LEFT HIP.
Patient problems: Insufficient Information
MAUDE report 11436304 ↗
Other Mesh, surgical, acetabular, hip, prosthesis devices
- NA 1011-40-030Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis13 reports
- NA 1011-40-025Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis13 reports
- NA 1011-40-020Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis11 reports
- NA 1011-40-040Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis11 reports
- NA 1011-40-035Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis9 reports
- NA 1011-40-015Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis8 reports
- NA 1011-71-000Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis4 reports
- NA 1011-02-501Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis3 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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