Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set Recalled by Baxter Healthcare Corporation Due to There were customer reports of separation between the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.
Affected Products
Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid Displacement, 5.7 " (14 cm), REF 7N8370K - Product Usage: intended for single patient use with a vascular access device for the administration of drugs and solutions without needles, thus eliminating the potential for needle-stick injuries during use.
Quantity: 66,800 units
Why Was This Recalled?
There were customer reports of separation between the tubing and Male Luer Lock Adaptor.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report