Bayer Medical Care, Inc. Avanta Multi-Patient Administration Tube Sets ) used recall: Supplier changes resulted in a fit issue with the Contrast Flow Control Valve
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.
The hazard: Fall or tip-over hazard
A fall or tip-over risk prompted this notice. With furniture, the typical victim is a toddler who used a drawer as a step.
What the notice says: 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.
Why it matters: The product can tip, collapse or give way under normal use. Furniture tip-overs in particular kill and injure young children, usually when a child climbs on an open drawer.
Symptoms and when to call a doctor
After a fall or a tip-over involving a child, watch for a headache that gets worse, repeated vomiting, drowsiness that is hard to rouse, confusion, unequal pupils, clear fluid from the nose or ear, or a seizure, and call 911 if any of these appear. Any fall onto the head in a baby under one, or any loss of consciousness at any age, needs to be assessed the same day.
This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.
Recall details
- Recall number
- Z-2296-2026
- Published
- June 10, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Bayer Medical Care, Inc.
- Product type
- Medical devices
- Units affected
- 11,300 units (1650 US, 9650 OUS)
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Catalog number: AVA 500 MPAT (Part 2 of 2) Affected material numbers: 87629007, 60729458, 86566648; Affected batch numbers: 251702, 252302, 252502, 252602, 252702, 252802, 253304, 253702, 253704, 253804, 254202, 254304, 254704, 254802;
Products covered by this recall
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
Check your product
The notice names 10 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Lot or batch code
Usually ink-stamped near the seam, the cap or the bottom of the pack.
- 251702
- 252302
- 252502
- 252602
- 252702
- 252802
- 253304
- 253702
- 253704
Model or item number
On the rating label, the box or the instruction sheet.
- AVA 500 MPAT
Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Fall
Bayer Medical Care, Inc. — A fall or tip-over risk prompted this notice. With furniture, the typical victim is a toddler who used a drawer as a step.
- Stop using the product and, if it is furniture, move it out of a child’s room until the remedy is done.
- Anchor tall furniture to the wall with a tip-over restraint — this is worth doing for every chest and bookcase in the house, not just this one.
- Keep TVs, toys and anything else tempting off the top of tall furniture, because that is what draws a child to climb.
- Inspect similar units from the same range, since a weak joint or fastener usually affects a whole production run.
If the claim stalls
Most recall claims are paid without argument. The ones that stall usually stall for a reason you can fix.
- Check you used the recall channel rather than ordinary customer support — the two queues rarely talk to each other.
- Paid by card? A chargeback for goods that are unfit for sale is a legitimate fallback once the company has had a fair chance.
- Send the photos they asked for in the format they asked for. A missing date code is the single commonest reason a claim sits unprocessed.
- Give it ten working days, then chase in writing and quote your claim reference.
Company contact: Bayer Medical Care, Inc. — 1 Bayer Dr, Indianola, PA, 15051-9702
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Bayer Medical Care, Inc. medical devices recalled?
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. 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…
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 251702, 252302, 252502; model number AVA 500 MPAT. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Stop using the product and, if it is furniture, move it out of a child’s room until the remedy is done.
Can I get my money back?
Check you used the recall channel rather than ordinary customer support — the two queues rarely talk to each other.
Where was the recalled product sold?
It was distributed nationwide.
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