InjuryKWD
FOREFOOT INTERNAL BRACE IMPLANT
Received Aug 16, 2019 · Event occurred Aug 9, 2019
Report MW5089117 · MDR key 8906408
Device
Generic name
Prosthesis, Toe, Hemi,phalangeal
Manufacturer
Arthrex, Inc.Model number
AR-1530-CPLot number
10298681
Product problems
- Break
- Detachment of Device or Device Component
Patient
69 YR
- Foreign Body In Patient
- Foreign Body In Patient
Narrative
Description of Event or Problem
WHEN USING THE FOREFOOT INTERNAL BRACE IMPLANT SYSTEM, A PIECE OF ONE OF THE INSTRUMENTS BROKE OFF IN THE PT'S FOOT. X-RAY OF THE FOOT WAS DONE, THE PIECE WAS UNABLE TO BE SEEN IN THE FOOT. FDA SAFETY REPORT ID# (B)(4).