M2A MAGNUM HIP SYSTEM 139252Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00880304428041), received between Mar 4, 2022 and Mar 4, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Material Erosion” (1 report).
1 other recall cover devices cleared under the same FDA submission (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
Device problems
- Material Erosion1
Patient problems
- Metal Related Pathology1
- Muscle/Tendon Damage1
- Swelling/ Edema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 4, 2022Material Erosion; Material Erosion
IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO ELEVATED METAL IONS, EFFUSION AND ADVERSE LOCAL TISSUE REACTION (ALTR) APPROXIMATELY 13 YEARS POST IMPLANTATION. DURING THE REVISION, AN ABDUCTOR TEAR AND TROCHANTERIC BURSA METAL DEBRIS WERE NOTED. METAL DEBRIS NOTED TO THE POSTERIOR CAPSULE AND BENEATH THE GREATER TROCHANTER. THE HEAD AND TAPER ADAPTER WERE EXCHANGED WITHOUT COMPLICATIONS. FEMORAL HEAD TRUNNION HAD <20% AREA OF DULLING. THE STEM AND CUP REMAINED IMPLANTED. IT WAS NOTED THE STABILITY CHECK SHOWED NO STABILITY POSTERIORLY AND ANTERIORLY. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Metal Related Pathology; Muscle/Tendon Damage; Swelling/ Edema
MAUDE report 13666916 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K101336. One submission often covers many models, so check the product and lot details in each record.
- Z-1465-2013 · Apr 26, 2013 · TerminatedActive Articulation E1. Intended for use with either primary or revision hip arthroplasty.
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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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