FDAClass IIOctober 1, 2025

Baster Continu-Flo Solution Set recall

Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519…

Why was Baster Continu-Flo Solution Set recalled?

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 00085412048994, Lot Number R24I20079, Exp. 9/21/2026

Product
Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519…
Recalling firm
Baxter Healthcare Corporation
Quantity
14400 units
Distribution
US Nationwide distribution.
Recall date
October 1, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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