Permobil: Medical Device Recall in 2023 - (Recall #: Z-2004-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

PushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D, MX2-33P, MX2-33PK, MX2-33S, MX2-150, MX2-167, MX2-32D); a wearable watch that communicates with a SmartDrive Power Assist Device via the SmartDrive MX2+ Application

Product Classification:

Class II

Date Initiated: May 10, 2023

Date Posted: July 5, 2023

Recall Number: Z-2004-2023

Event ID: 92250

Reason for Recall:

When multiple processes are running on the watch's Central Processing Unit (CPU), the application may fail unexpectedly. If this happens, the motor on the power assist device continues to run and the user may not be able to stop the device using tap gestures.

Status: Ongoing

Product Quantity: 18,905 units

Code Information:

All units with software versions 1.0.00 to 1.0.04

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated