PlainRecalls
FDA Devices Moderate Class II Terminated

MOMENTUM X4 CRT-D, Model G138, Sterile.

Reported: November 15, 2017 Initiated: October 4, 2017 #Z-0080-2018

Product Description

MOMENTUM X4 CRT-D, Model G138, Sterile.

Reason for Recall

The devices have an incorrect firmware configuration.

Details

Units Affected
4 devices
Distribution
The devices were distributed to medical facilities located in MN and OH. There was no foreign/government/military distribution.
Location
Saint Paul, MN

Frequently Asked Questions

What product was recalled?
MOMENTUM X4 CRT-D, Model G138, Sterile.. Recalled by Boston Scientific Corporation. Units affected: 4 devices.
Why was this product recalled?
The devices have an incorrect firmware configuration.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 15, 2017. Severity: Moderate. Recall number: Z-0080-2018.