Boston Scientific CRM Corp: Medical Device Recall in 2013 - (Recall #: Z-1339-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

LATITUDE¿ Patient Management System, Model 6488, Version 7.3. The LATITUDE Patient Management system is intended for use to remotely communicate with a compatible Boston Scientific pulse generator and transfer data to a central database.

Product Classification:

Class II

Date Initiated: April 10, 2013

Date Posted: May 29, 2013

Recall Number: Z-1339-2013

Event ID: 65096

Reason for Recall:

Boston Scientific CRM is conducting a recall on the LATITUDE Patient Management System Model 6488 Version 7.3 because between March 4 and 27, 2013, a Siebel release caused ~5000 distributed PMR clinic faxes to display with illegible characters and not the required, Patient non-compliance information that was intended.

Status: Terminated

Product Quantity: 1

Code Information:

n/a

Distribution Pattern:

Nationwide Distribution including DC and PR

Voluntary or Mandated:

Voluntary: Firm initiated