# FDA recall Z-1947-2020

> **Sunrise Medical (US) LLC** · Class II · device recall initiated 2020-02-13.

## Product

Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is controlled by Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966).

## Reason for recall

Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.

## Distribution

Distributed to US Consignee in MT.

## Key facts

- **Recall number:** Z-1947-2020
- **Recalling firm:** Sunrise Medical (US) LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-13
- **Report date:** 2020-05-20
- **Termination date:** 2021-04-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fresno, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1947-2020

## Citation

> AI Analytics. FDA recall Z-1947-2020. Retrieved 2026-07-07 from https://api.ai-analytics.org/recall/Z-1947-2020. Source: US FDA. Licensed CC0.

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