MalfunctionOGJ
ARROW CONTINUOUS NERVE BLOCK KIT
Received Mar 19, 2015 · Event occurred Feb 20, 2015
Report 1036844-2015-00073 · MDR key 4620143
Device
Product problems
- Kinked
Patient
Not reported
- No Consequences Or Impact To Patient
Narrative
Additional Manufacturer Narrative
(B)(4). IT IS UNKNOWN IF THE DEVICE SAMPLE IS AVAILABLE FOR EVALUATION.
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.