Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter Non-DEHP Micro-Volume Extension Set Recalled by Baxter Healthcare Corp. Due to Some of the individual extension set packages were...
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 Corp. directly.
Affected Products
Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single use nonpyrogenic fluid pathway; 50 sets per case; For the administration of drugs and solutions to a patient's vascular system through a vascular access device.
Quantity: 15,257 units
Why Was This Recalled?
Some of the individual extension set packages were improperly sealed, compromising the sterility of the product.
Where Was This Sold?
This product was distributed to 15 states: FL, GA, IL, KS, KY, MI, MO, NC, ND, OH, PA, SC, TN, TX, WV
About Baxter Healthcare Corp.
Baxter Healthcare Corp. has 126 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report