Siemens Medical Solutions USA, Inc 2024-01-17 Health serious FDA
Health · FDA · Recall #FDA-Z-0683-2024
Sensis Vibe Hemo Recall
Issued January 17, 2024 · Siemens Medical Solutions USA, Inc
In January 2024, Siemens Medical Solutions USA, Inc recalled the Sensis Vibe Hemo, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The possibility of the Sensis documentation functionality application to crash.
What you should do
- 1 Stop using Sensis Vibe Hemo right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Siemens Medical Solutions USA, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Siemens Medical Solutions USA, Inc
- Category
- Health
- Recall date
- January 17, 2024
- Units affected
- Not reported
- Sold at
- Domestic: CA, CT, & FL.
- Recall number
- FDA-Z-0683-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Siemens Medical Solutions USA, Inc has 17 recalls in our database, including 2 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.