NA 9626-45-000Recalls & reported problems
Depuy (Ireland) · MARATHON XLPE CEMENTED CUP 45mm TRIAL CUP · Class 1
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 10603295243649), received between Jun 17, 2021 and Apr 4, 2022 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Naturally Worn” (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.
Most reported problems
Device problems
- Naturally Worn4
- Material Twisted/Bent3
- Crack1
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 4, 2022Naturally Worn; Naturally Worn
THE HOLES ARE DAMAGED AND THE HANDLE NO LONGER HOLDS THE TRIAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13994095 ↗MalfunctionFeb 7, 2022Crack; Crack
IT WAS REPORTED THAT THE 45MM CUP TRIAL OFF OUR MARATHON TRAY IS DAMAGED AND BROKEN. THEY NOTICED IT BEFORE SURGERY HAD COMMENCED. NOT PRESENT DURING THE CASE BUT NO HARM TO PATIENT OR DELAY IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13470723 ↗MalfunctionJun 17, 2021Material Twisted/Bent; Naturally Worn; Material Twisted/Bent; Naturally Worn
NO IMPACT ON PATIENT NO DELAY TO SURGERY. WORN ITEMS ¿ AL BEEN IN SERVICE CIRCA 8 YEARS AND HAVE WORN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12019081 ↗MalfunctionJun 17, 2021Material Twisted/Bent; Naturally Worn; Material Twisted/Bent; Naturally Worn
NO IMPACT ON PATIENT. NO DELAY TO SURGERY. WORN ITEMS ¿ AL BEEN IN SERVICE CIRCA 8 YEARS AND HAVE WORN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12019062 ↗MalfunctionJun 17, 2021Material Twisted/Bent; Naturally Worn; Material Twisted/Bent; Naturally Worn
NO IMPACT ON PATIENT. NO DELAY TO SURGERY. WORN ITEMS: AL BEEN IN SERVICE CIRCA 8 YEARS AND HAVE WORN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12019061 ↗
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- 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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