PINNACLE GRIPTION 1217-31-044Recalls & reported problems
Depuy Orthopaedics, Inc. · PINNACLE 100 ACETABULAR SHELL GRIPTION 100 44mm OD · Class 2 · Implant
All models of PINNACLE GRIPTION (57)
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 10603295010166), received between Mar 17, 2022 and Jun 7, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 18, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated2
- Noise, Audible1
Patient problems
- Insufficient Information1
- Joint Laxity1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 7, 2022Device Dislodged or Dislocated; Noise, Audible; Device Dislodged or Dislocated; Noise, Audible
PATIENT ACCOUNT OF EXPERIENCE: I FELT AN IMBALANCE WITH PAIN IN THE LEG WHERE I WAS PLACED THE PROSTHESIS, AFTER THE PAIN A SQUEAK HAS INCREASED, I WENT TO CONSULT WITH THE TREATING DOCTOR AND HIS DIAGNOSIS IS THAT THE PROSTHESIS HAD A BREAK IN THE POLYETHYLENE PART, (THAT THE PIECE CAME OUT WRONG). HOSPITAL REPORT: HEREBY INFORM YOU THAT THE PATIENT UNDERWENT SURGICAL TREATMENT; THE SURGERY WAS LEFT HIP TOTAL ARTHROPLASTY AND WAS PERFORMED WITHOUT COMPLICATIONS. THE PROSTHESIS THAT WAS PLACED IN THIS PROCEDURE WAS JOHNSON'S PROSTHESIS, SUMMIT STEM PINACLE ACETABULUM, AND CORAIL.
Patient problems: Joint Laxity; Pain
MAUDE report 14621234 ↗InjuryMar 17, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT HAD A TOTAL HIP DONE AT (B)(6) ON (B)(6) 2022. SOMETIME BETWEEN THEN AND (B)(6) THE LINER DISASSOCIATED FROM THE CUP. THE SURGEON NOTICED IT ON X-RAY WHEN SHE WAS IN FOR HER 2 WEEKS FOLLOW UP AND SHE WAS IMMEDIATELY BOOKED FOR REVISION SURGERY ON (B)(6) 2022 THE SURGEON WOULD LIKE THE LINER ANALYSED AND THE MECHANISM OVER FAILURE LOOKED INTO. DOI: (B)(6) 2022, DOR: (B)(6) 2022, AFFECTED SIDE: LEFT HIP AFFECTED.
Patient problems: Insufficient Information
MAUDE report 13800697 ↗
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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