Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LATITUDE¿ Patient Management System Recalled by Boston Scientific CRM Corp Due to Boston Scientific CRM is conducting a recall on...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Boston Scientific CRM Corp directly.
Affected Products
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.
Quantity: 1
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Boston Scientific CRM Corp
Boston Scientific CRM Corp has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report