MalfunctionMDM
ARTHREX SCORPION-MULTIFIRE NEEDLE
Received Mar 9, 2022 · Event occurred Feb 15, 2022
Report MW5107999 · MDR key 13720508
Device
Generic name
Instrument, Manual, Surgical, General Use
Manufacturer
Arthrex GmbhModel number
AR-13995N/Catalog number
AR-13995N/
Lot number
14549405
Product problems
- Break
Patient
70 YR · Female
- Insufficient Information
- Insufficient Information
Narrative
Description of Event or Problem
ARTHREX SCORPION-MULTIFIRE NEEDLE WITH REFERENCE: AR-13995N/ LOT 14549405 BROKE WHILE IN USE DURING SURGERY. FDA SAFETY REPORT ID # (B)(4).