Restoration 504-02-68F-RRecalls & reported problems
Howmedica Osteonics Corp. · Anatomic Hemispherical Shell · Class 2 · Implant
All models of Restoration (86)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327012514), received between Jun 27, 2019 and Dec 19, 2022 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Component Misassembled” (4 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 18, 2026.
Most reported problems
Device problems
- Component Misassembled4
- Packaging Problem4
- Device Dislodged or Dislocated1
- Loss of Osseointegration1
- Migration1
Patient problems
- No Consequences Or Impact To Patient4
- No Known Impact Or Consequence To Patient4
- Ambulation or Postural Difficulties1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryDec 19, 2022Loss of Osseointegration; Device Dislodged or Dislocated; Migration; Loss of Osseointegration; Device Dislodged or Dislocated; Migration
IT WAS REPORTED THE PATIENT'S RIGHT HIP WAS REVISED. NOTED ON THE PATIENT SPECIFIC REQUEST FORM: "RIGHT FAILED TOTAL HIP ARTHROPLASTY WITH ACETABULAR DESTRUCTION. LOOSENING OF THE RIGHT ACETABULUM STATUS POST 2 REVISION HIP ARTHROPLASTY. PROXIMAL LATERAL MIGRATION OF THE ACETABULAR COMPONENT. EXTENSIVE BONE LOSS."
Patient problems: Ambulation or Postural Difficulties
MAUDE report 16003421 ↗MalfunctionJul 24, 2019Packaging Problem; Component Misassembled; Packaging Problem; Component Misassembled
UPON INCOMING INSPECTION IT WAS NOTICED THAT THE PRODUCT WAS LOOSE IN PACKAGING. DEVICE HAS BEEN SHIPPED TO THE DECON LAB. NO FURTHER INFORMATION AVAILABLE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8821582 ↗MalfunctionJul 1, 2019Packaging Problem; Component Misassembled; Packaging Problem; Component Misassembled
UPON INCOMING INSPECTION IT WAS NOTICED THAT THE IMPLANTS WERE LOOSE IN PACKAGING. IMPLANTS HAVE BEEN SHIPPED TO THE DECON LAB. NO FURTHER INFORMATION AVAILABLE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8748270 ↗MalfunctionJun 27, 2019Packaging Problem; Component Misassembled; Packaging Problem; Component Misassembled
UPON INCOMING INSPECTION IT WAS NOTICED THAT THE IMPLANTS WERE LOOSE IN PACKAGING. THE IMPLANTS HAVE BEEN SHIPPED TO THE DECON LAB. NO FURTHER INFORMATION AVAILABLE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8738770 ↗MalfunctionJun 27, 2019Packaging Problem; Component Misassembled; Packaging Problem; Component Misassembled
UPON INCOMING INSPECTION IT WAS NOTICED THAT THE IMPLANT WAS LOOSE IN PACKAGING. IMPLANTS HAVE BEEN SHIPPED TO THE DECON LAB. NO FURTHER INFORMATION AVAILABLE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8738433 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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