InjuryKWD

HEMICAP

Received Apr 27, 2026 · Event occurred Apr 15, 2026

Report 3004154314-2026-00002 · MDR key 25001638

Device

Generic name

Prosthesis, Toe, Hemi-, Phalangeal

Manufacturer

Arthrosurface, Inc.

Product problems

Prophylactic removal due to corrective action

Patient

NA · Unknown

Pain

Narrative

Additional Manufacturer Narrative

THE COMPLAINANT MADE NO INDICATION OF ANY ARTHROSURFACE DEVICE MALFUNCTION OR DEFICIENCY RELATED TO THE IDENTITY, QUALITY, DURABILITY, RELIABILITY, SAFETY, EFFECTIVENESS OR DEVICE PERFORMANCE CONTRIBUTING TO THE ADVERSE EVENT.

Description of Event or Problem

A COMPLAINT WAS INITIATED ON (B)(6) 2026 NOTIFYING ARTHROSURFACE OF AN UPCOMING REMOVAL SURGERY FOR PATIENT PAIN. THE REMOVAL TOOK PLACE ON (B)(6) 2026. REMOVAL SURGERY CONFIRMED ON (B)(6) 2026.