# FDA recall Z-2626-2017

> **EOS Imaging** · Class II · device recall initiated 2017-05-30.

## Product

ROTH MOBELI Grab Handles used with EOS System: MOBELI Stabi Vario Grab Handle, ROTH Catalogue Number 14002 96 S, EOS Imaging Catalogue Number 9000111773; and MOBELI Dual Grip Grab Handle, ROTH Catalogue Number 14002 25 S, EOS Imaging Catalogue Number 9000111774.

## Reason for recall

ROTH MOBELI grab handles could detach and patient could fall if the EOS system operator does not follow instructions. Before each use, the operator must examine the vacuum safety indicator to check the vacuum is monitored and sufficient and the grab handle correctly attached.  Do not use grab handles to help patient up. The handles are only for stabilizing the patients hand or arm in the EOS cabin.

## Distribution

US Distribution to the states of : Pennsylvania, Massachusetts, Minnesota, Alabama, Michigan, Texas and  Washington.

## Key facts

- **Recall number:** Z-2626-2017
- **Recalling firm:** EOS Imaging
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-30
- **Report date:** 2017-07-05
- **Termination date:** 2018-10-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Paris, N/A, France

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2626-2017

## Citation

> AI Analytics. FDA recall Z-2626-2017. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2626-2017. Source: US FDA. Licensed CC0.

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