PROFEMUR® Modular Femoral Neck
Received Jul 27, 2026
Report 3010536692-2026-00287 · MDR key 50027777
Device
Generic name
Hip Component
Manufacturer
Microport Orthopedics Inc.Model number
PHA01202Catalog number
PHA01202
Lot number
0111291071
Product problems
- Insufficient Device Problem Information
Patient
49 YR · Female
- Metal Related Pathology
Narrative
Additional Manufacturer Narrative
MicroPort was made aware of this revision from the United Kingdom National Joint Registry. Reference investigation memorandum for full information. The indications for revision are known inherent risks of the device and/or procedure. Furthermore, there were no increases in hazard and harm risk levels identified for these product families. Therefore, no additional action is required.
Description of Event or Problem
Allegedly, patient was revised due to Adverse Soft Tissue Reaction to Particulate Debris.SRNJR Number: (b)(6).Side: L.Gender: F.