Baxter Healthcare Corporation 2024-01-17 Health serious FDA
Health · FDA · Recall #FDA-Z-0663-2024
Baxter Flo-Thru Intraluminal Shunt, Product Codes: a) Product Code FT12100, 1.00… Recall
Issued January 17, 2024 · Baxter Healthcare Corporation
In January 2024, Baxter Healthcare Corporation recalled the Baxter Flo-Thru Intraluminal Shunt, Product Codes: a) Product Code FT12100, 1.00…, 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
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
What you should do
- 1 Stop using Baxter Flo-Thru Intraluminal Shunt, Product Codes: a) Product Code FT12100, 1.00… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Baxter Healthcare Corporation 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
- Baxter Healthcare Corporation
- Category
- Health
- Recall date
- January 17, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-0663-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Baxter Healthcare Corporation has 36 recalls in our database, including 5 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.