Bayer Medical Care, Inc. 2026-06-10 Health serious FDA
Health · FDA · Recall #FDA-Z-2296-2026
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the… Recall
Issued June 10, 2026 · Bayer Medical Care, Inc.
In June 2026, Bayer Medical Care, Inc. recalled the Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.
What you should do
- 1 Stop using Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Bayer Medical Care, 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
- Bayer Medical Care, Inc.
- Category
- Health
- Recall date
- June 10, 2026
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, DE, FL, IA, IL, IN, KS, KY, LA, MA, MD, ME, MO, NC, NY
- Recall number
- FDA-Z-2296-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Bayer Medical Care, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.