# FDA recall Z-0047-2018

> **Siemens Medical Solutions USA, Inc.** · Class II · device recall initiated 2017-09-18.

## Product

Torque wrench used on the bolts for the Symbia T2 model 10275008, Symbia Intevo Excel model 10764801, Symbia Intevo 16 model 10764804, Symbia Evo model 10910500, and Symbia Evo Excel model 10910501 devices.

## Reason for recall

The torque wrench used to tighten system bolts during installation was found to be out of tolerance

## Distribution

Distribution was made to medical facilities located in CA, FL, GA, LA, NY, PA, and TN.  There was government distribution but no foreign/military distribution.

## Key facts

- **Recall number:** Z-0047-2018
- **Recalling firm:** Siemens Medical Solutions USA, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-18
- **Report date:** 2017-11-01
- **Termination date:** 2017-12-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hoffman Estates, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0047-2018

## Citation

> AI Analytics. FDA recall Z-0047-2018. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-0047-2018. Source: US FDA. Licensed CC0.

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