M2a Magnum™ Hip System US157852Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304993501), received between Dec 10, 2020 and Dec 10, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K042037, K101336); they may or may not involve this specific model.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 10, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT A HIP REVISION APPROXIMATELY 1 MONTH POST IMPLANTATION AND A SECOND REVISION APPROXIMATELY 1 MONTH AFTER THAT DUE TO DISLOCATION AND DISSOCIATION OF THE HEAD AND BEARING. IT WAS REPORTED THAT THE PATIENT EXPERIENCED A FALL. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME

  Patient problems: Fall; Joint Dislocation

  MAUDE report 10984094 ↗
• InjuryDec 10, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT A HIP REVISION APPROXIMATELY 1 MONTH POST IMPLANTATION DUE TO DISLOCATION AND DISSOCIATION OF THE HEAD AND BEARING. IT WAS REPORTED THAT THE PATIENT EXPERIENCED A FALL. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Fall; Joint Dislocation

  MAUDE report 10983993 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042037, K101336. One submission often covers many models, so check the product and lot details in each record.

• Z-1465-2013 · Apr 26, 2013 · Terminated
  Active Articulation E1. Intended for use with either primary or revision hip arthroplasty.