FDAFDA · Food and drugs·Recall number Z-0683-2024
Sensis Vibe Hemo
Published January 17, 2024 · Recall initiated: November 29, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The possibility of the Sensis documentation functionality application to crash.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- Domestic: CA, CT, & FL.
- Lot
- Model No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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