# FDA recall Z-0006-2018

> **Permobil, Ab** · Class II · device recall initiated 2017-09-01.

## Product

Electric Wheelchair bases:  a) C300   b) C350   c) C400   d) C500

## Reason for recall

There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.

## Distribution

Nationwide and Australia, Benelux, Canada, Denmark, Finland, France, Germany, Israel, Norway, Sweden, and UAE

## Key facts

- **Recall number:** Z-0006-2018
- **Recalling firm:** Permobil, Ab
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-01
- **Report date:** 2017-10-11
- **Termination date:** 2021-05-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Timra, N/A, Sweden

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0006-2018

## Citation

> AI Analytics. FDA recall Z-0006-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0006-2018. Source: US FDA. Licensed CC0.

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