PINNACLE 1219-32-062Recalls & reported problems
Depuy Orthopaedics, Inc. · PINNACLE HIP SOLUTIONS MARATHON POLYETHYLENE ACETABULAR LINER NEUTRAL 32mm ID 62mm OD · Class 2 · Implant
All models of PINNACLE (182)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295013952), received between Nov 3, 2020 and Nov 24, 2020 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
- Naturally Worn1
- Noise, Audible1
Patient problems
- No Code Available2
- Pain2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Deformity/ Disfigurement1
- Discomfort1
- Joint Dislocation1
- Limited Mobility Of The Implanted Joint1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryNov 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT HAD PAINFUL HIP. SURGEON EXPLANTED METAL HEAD AND LINER REVISING WITH CERAMIC REV AND ALTRX. DOI: UNKNOWN, DOR: (B)(6) 2020, AFFECTED SIDE: LEFT HIP.
Patient problems: Deformity/ Disfigurement; Pain
MAUDE report 10896281 ↗InjuryNov 9, 2020Device Dislodged or Dislocated; Noise, Audible; Device Dislodged or Dislocated; Noise, Audible
SURGEON REPORTED TO NCA (BFARM): "HIP-TEP LEFT SIDE ON (B)(6) 2013 IN OUR HOSPITAL. SINCE (B)(6)2020, AFTER A ROTATIONAL MOVEMENT WHILE WORKING IN THE GARDEN, PATIENT WAS EXPERIENCING INCREASING PAIN AND DISCOMFORT IN THE LEFT HIP JOINT. AFTER THIS, HE EXPERIENCED SQUEAKING NOISES IN THE LEFT JOINT PLUS FUNCTIONAL RESTRICTMENTS AND PAIN UNDER LOAD. HIP-TEP RIGHT SIDE IN 3/2007; CONTENT WITH THIS ONE. THE X-RAY EXAMINATION INDICATED A DISLOCATED INLAY OF THE HIP-TEP ON THE LEFT. REVISION OF LEFT HIP-TEP ON (B)(6) 2020."
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Discomfort; Joint Dislocation; Limited Mobility Of The Implanted Joint; No Code Available; Pain
MAUDE report 10808928 ↗InjuryNov 3, 2020Naturally Worn; Naturally Worn
THE PATIENT WAS REVISED DUE TO POLY WEAR. DOI: UNKNOWN; DOR: (B)(6) 2020; AFFECTED SIDE: RIGHT HIP.
Patient problems: No Code Available
MAUDE report 10778675 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page