# FDA recall Z-0036-2024

> **Getinge Usa Sales Inc** · Class II · device recall initiated 2023-09-06.

## Product

Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment.  Model Number: 7200.01F2

## Reason for recall

Under certain conditions, an issue might prevent the device from performing as intended. A specific sequence of commands on the control unit activates the traction drive and triggers an unintended driving (autodrive) of max. 7 sec. may result in the following reasonably foreseeable injury or damage to the health of patients and/or users

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0036-2024
- **Recalling firm:** Getinge Usa Sales Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-06
- **Report date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wayne, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0036-2024

## Citation

> AI Analytics. FDA recall Z-0036-2024. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-0036-2024. Source: US FDA. Licensed CC0.

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