FDA DeviceClass IINotable

FDA Recall: Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, im

Date: 2026-06-03
Brand: Medtronic Neuromodulation
Category: Medical Device
FDA Class: Class II

Description

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

Hazard

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

Remedy

31 units

View original recall →
Share:

Related Recalls

2026-06-03 · FDA_DEVICE
FDA Recall: Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, im
Medtronic Neuromodulation
2026-05-20 · FDA_DEVICE
FDA Recall: Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on
Medtronic Neuromodulation