MobiliT Cup HDM560Recalls & reported problems
Corin Ltd · MobiliT Cemented dual mobility acetabular cup – Dia. 60 · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05056139200830), received between Feb 5, 2026 and Feb 5, 2026 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 5, 2026Adverse Event Without Identified Device or Use Problem
MOBILIT REVISION OF THE CUP AND PE INSERT DUE TO INFECTION. NOTE: THE INSERT HDM260 IS NOT CLEARED IN THE USA.
Patient problems: Unspecified Infection
MAUDE report 24266879 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.