FDA Enforcement Class II Terminated

Boston Scientific, MRI PROPONENT" SR , REF L210 Pacemaker. These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary

Recall: Z-0620-2016 · Reported January 20, 2016

Enforcement

Recall Number
Z-0620-2016
Event ID
72855
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Boston Scientific Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
January 20, 2016
Initiation Date
December 10, 2015
Classification Date
January 8, 2016
Termination Date
March 8, 2016
Address
4100 Hamline Ave N, N/A, Saint Paul, MN, 55112-5700, United States

Description

Boston Scientific, MRI PROPONENT" SR , REF L210 Pacemaker. These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary

Reason

The literature packet packaged with the devices incorrectly describes the pacemaker as SR when it is actually a DR pacemaker or DR when it is actually a SR pacemaker.

Code Info

Serial numbers 702961, 702963, 705644, 705666, and 705947.

Distribution

International Distribution to countries of: COLOMBIA, JAMAICA, TRINIDAD & TOBAGO.

Quantity

5