• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of May 29, 2013

  • Print
  • Share
  • E-mail

Product Detail

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.
Recall Number Z-1339-2013
Classification Class II
Code Info n/a
Product Distributed Qty 1
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.

Event Detail

Event Id 65096
Product Type Devices
Status Ongoing
Recalling Firm Boston Scientific CRM Corp
City Saint Paul
State MN
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-04-10
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern Nationwide Distribution including DC and PR