InjuryJDI
UNK MODULAR ARCOS STEM
Received Jul 14, 2026
Report 0001825034-2026-02067 · MDR key 25816120
Device
Generic name
Prosthesis, Hip
Manufacturer
Zimmer Biomet, Inc.Catalog number
UNK MODULAR ARCOS STEM
Lot number
UNK
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Insufficient Information
Narrative
Additional Manufacturer Narrative
(B)(4). PROPOSED COMPONENT CODE: MECHANICAL (G04) - STEM. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED.
Description of Event or Problem
IT WAS REPORTED THAT A PATIENT UNDERWENT A LEFT HIP ARTHROPLASTY ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT WAS BEING CONSIDERED FOR A PATIENT-MATCHED IMPLANT DUE TO UNKNOWN REASONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.