# FDA recall Z-2005-2023

> **Permobil** · Class II · device recall initiated 2023-05-10.

## Product

PushTracker E3 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

## 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.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-2005-2023
- **Recalling firm:** Permobil
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-10
- **Report date:** 2023-07-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lebanon, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2005-2023

## Citation

> AI Analytics. FDA recall Z-2005-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2005-2023. Source: US FDA. Licensed CC0.

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