PINNACLE GRIPTION 1217-17-070Recalls & reported problems
Depuy Orthopaedics, Inc. · PINNACLE GRIPTION ACETABULAR SHELL REVISION (DPX) 70mm OD 64 LINER · 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 10603295009535), received between Jan 11, 2018 and Aug 27, 2018 — classified as 2 injuries.
The most frequently reported specific device problem is “Failure To Adhere Or Bond” (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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Failure To Adhere Or Bond1
Patient problems
- Inadequate Osseointegration1
- No Code Available1
- No Known Impact Or Consequence To Patient1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 27, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PPF AND STICKER SHEETS RECEIVED. THERE IS NO ALLEGATION. IT WAS INDICATED THAT PATIENT HAD A SECOND REVISION ON (B)(6) 2014. THE CUP, HEAD AND LINER WERE REMOVED. DOI: (B)(6) 2011; DOR: (B)(6) 2014; (LEFT HIP).
Patient problems: No Code Available; No Known Impact Or Consequence To Patient; Pain
MAUDE report 7817871 ↗InjuryJan 11, 2018Failure To Adhere Or Bond; Failure To Adhere Or Bond
CLINICAL DER RECEIVED. AE RECEIVED FOR LOOSENED ACETABULAR CUP. DEPUY CEMENT IS USED. EVENT DOES MEET THE DEFINITION OF SERIOUS AND IS CONSIDERED MILD. EVENT IS DEFINITELY RELATED TO DEVICE AND DEFINITELY NOT RELATED TO PROCEDURE. AWAITING REVISION. (B)(6) 2016 (HEAD, LINER AND CUP); AE: (B)(6) 2017; RIGHT HIP.
Patient problems: Inadequate Osseointegration
MAUDE report 7182378 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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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