MalfunctionOGJ
ARROW CONTINUOUS NERVE BLOCK KIT
Received Mar 20, 2015 · Event occurred Feb 20, 2015
Report 1036844-2015-00074 · MDR key 4623980
Device
Product problems
- Kinked
Patient
Not reported
- No Consequences Or Impact To Patient
Narrative
Description of Event or Problem
THE CUSTOMER ALLEGES THAT WHILE USING THE FLEX BLOCK KIT; THE CATHETER KINKED INSIDE THE NEEDLE. NO PATIENT INJURY OR HARM REPORTED.
Additional Manufacturer Narrative
(B)(4). IT IS UNKNOWN IF THE DEVICE SAMPLE IS AVAILABLE FOR EVALUATION.