PINNACLE 2218-40-060Recalls & reported problems
Depuy (Ireland) · PINNACLE ACETABULAR LINER TRIAL NEUTRAL 40ID x 60OD · Class 1
All models of PINNACLE (198)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295429999), received between Nov 29, 2021 and Apr 13, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility2
- No Apparent Adverse Event2
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 13, 2026No Apparent Adverse Event
IT WAS REPORTED THAT THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24857410 ↗MalfunctionMar 26, 2026No Apparent Adverse Event
IT WAS REPORTED THAT THE IMPACTED PRODUCTS HAD AN UNKNOWN ALLEGATION. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24699891 ↗MalfunctionMar 16, 2022Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE 40MM X 60MM NEUTRAL LINER TRIAL WAS USED IN HIP ARTHROPLASTY CASE AND WHEN THE INSTRUMENTS CAME OUT OF THE WASH, THE LINER TRIAL WAS MISSING THE THREADED CONNECTING SCREW THAT LOCKS IT INTO THE CUP/CUP TRIAL. IT APPEARS IT WAS DISASSEMBLED FOR CLEANING PURPOSES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13790255 ↗MalfunctionNov 30, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE LINER TRIALS FOR THE SIZE 40 WERE NOT SEATING PROPERLY. SURGEON REQUESTS NEW SET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12897852 ↗MalfunctionNov 29, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE LINER TRIAL WOULDN'T SEAT IN THE CUP AND THE SURGEON ASKED TO GET A SET IN THAT WOULD WORK. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12883247 ↗
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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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