CRE PRO

Additional Manufacturer Narrative

BLOCK B3: APPROXIMATED BASED ON THE DATE THE MANUFACTURER BECAME AWARE OF THE EVENT. BLOCK E: THIS EVENT WAS REPORTED BY THE SALES REPRESENTATIVE. THE HEALTHCARE FACILITY IS: (B)(6). BLOCK H6: IMDRF DEVICE CODE (B)(4). CAPTURES THE REPORTABLE EVENT OF TEAR, RIP, HOLE IN DEVICE PACKAGING.

Description of Event or Problem

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A CRE PRO WIREGUIDED DILATATION BALLOON WAS RECEIVED BY THE CUSTOMER ON AN UNKNOWN DATE. IT WAS REPORTED THAT THE PRODUCTS WERE REPORTED AS DAMAGED UPON RECEIPT BY THE CUSTOMER. THE PATIENT WAS NOT PRESENT AT THE TIME OF THE EVENT, AND THE PRODUCT WAS NOT USED IN A PROCEDURE.