MalfunctionMDM
UNK
Received Mar 25, 2026 · Event occurred Mar 4, 2026
Report 1220246-2026-01648 · MDR key 24689254
Device
Generic name
Manual Instr, General Surgical
Manufacturer
Arthrex, Inc.Model number
UNKCatalog number
UNK
Lot number
UNK
Product problems
- Defective Device
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
INVESTIGATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE PROVIDED UPON AVAILABILITY OF ADDITIONAL INFORMATION.
Description of Event or Problem
ON (B)(6) 2026, IT WAS REPORTED BY A DISTRIBUTOR VIA (B)(4) THAT AN AR-13999MF FASTPASS SCORPION HAD A DAMAGED NEEDLE. THIS WAS DISCOVERED AFTER USE WITH NO PATIENT HARM.