# FDA recall Z-0683-2024

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2023-11-29.

## Product

Sensis Vibe Hemo

## Reason for recall

The possibility of the Sensis documentation functionality application to crash.

## Distribution

Domestic: CA, CT, & FL.

## Key facts

- **Recall number:** Z-0683-2024
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-29
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0683-2024

## Citation

> AI Analytics. FDA recall Z-0683-2024. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0683-2024. Source: US FDA. Licensed CC0.

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