PINNACLE 2218-60-051Recalls & reported problems
Depuy (Ireland) · PINNACLE DUAL MOBILITY LINER TRIAL 60/51 · Class 1
All models of PINNACLE (198)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295520597), received between Aug 3, 2021 and Dec 4, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break4
- Crack2
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Insufficient Information1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 4, 2025Break; Break
IT WAS REPORTED THAT SURGEON TIGHTENED THE TRIAL LINER INTO THE IMPLANT AND IT BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23715972 ↗MalfunctionNov 19, 2025Break; Break
IT WAS REPORTED THAT DURING A TOTAL HIP REPLACEMENT PROCEDURE, THERE WAS SLICES AND CHUNKS OBSERVED ON OUTER RIM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23597516 ↗MalfunctionSep 6, 2024Break; Break
IT WAS REPORTED THAT DUAL MOBILITY LINER TRIAL BROKE EITHER IN WASHER OR WAS DROPPED IN CENTRAL STERILE DEPARTMENT. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: Insufficient Information
MAUDE report 20155304 ↗MalfunctionAug 7, 2023Crack; Crack
IT WAS REPORTED THAT THREADED PART ON THE 50/43 LINER BROKE. THE 60/51 LINER TRIAL IS CRACKED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17470706 ↗MalfunctionFeb 10, 2022Crack; Crack
IT WAS REPORTED THAT THE SIZE 60 DM LINER WAS CRACKED DURING THE SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13507522 ↗MalfunctionAug 3, 2021Break; Break
IT WAS REPORTED THAT THE LIP OF THE LINER BROKE DURING TRIAL REDUCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12267056 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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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