NAVIFLEX? PUSHER
Received Jul 15, 2026 · Event occurred Jun 1, 2026
Report 3005099803-2026-02853 · MDR key 25834103
Device
Generic name
Catheter, Biliary, Diagnostic
Manufacturer
Boston Scientific CorporationModel number
M00535030Catalog number
M00535030
Lot number
0038904309
Product problems
- Device Markings/Labelling Problem
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
NOTE: RELATED NAVIFLEX LONG WIRE PUSHER COMPLAINTS ARE REPORTED UNDER RECORDS (B)(4). IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT LABELING DISCREPANCY WAS IDENTIFIED: THE PACKAGE WAS LABELED AS A LONG WIRE PUSHER; HOWEVER, THE DEVICE INSIDE WAS A SHORT WIRE PUSHER. IT WAS ALSO DETERMINED THAT THE PRODUCT OPENED HAD A SIDE-HOLE FEATURE. THERE WAS NO PATIENT INVOLVEMENT.
Additional Manufacturer Narrative
BLOCK B3: APPROXIMATED BASED ON THE DATE THE MANUFACTURER BECAME AWARE OF THE EVENT. BLOCK H6: IMDRF DEVICE CODE A2101 CAPTURES THE REPORTABLE EVENT OF DEVICE LABELING ISSUE.