Sensis Vibe Hemo
Reported: January 17, 2024 Initiated: November 29, 2023 #Z-0683-2024
Product Description
Sensis Vibe Hemo
Reason for Recall
The possibility of the Sensis documentation functionality application to crash.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 331 units
- Distribution
- Domestic: CA, CT, & FL.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
Sensis Vibe Hemo. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 331 units.
Why was this product recalled? ▼
The possibility of the Sensis documentation functionality application to crash.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 17, 2024. Severity: Moderate. Recall number: Z-0683-2024.
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