St. Jude Medical, Inc.: Medical Device Recalls in 2014

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by St. Jude Medical, Inc. in 2014. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Percutaneous Trial Lead Kit Model 3086 (8 ch percutaneous lead). Used as part of the St. Jude Medical Neurostimulation system indicated for Spinal Chord Stimulation.
Percutaneous Trial Lead Kit Model 3046 (4 ch percutaneous lead). Used as part of the St. Jude Medical Neurostimulation system indicated for Spinal Chord Stimulation.