Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Q2 Multiport Extension set Recalled by Quest Medical, Inc. Due to For administration of intravenous fluids to a patient...
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 Quest Medical, Inc. directly.
Affected Products
Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets with a multiport IV manifold and integrated back-check valves, pre-attached needleless injection sites, drip chamber and roller clamps.
Quantity: 17,700 units
Why Was This Recalled?
For administration of intravenous fluids to a patient s vascular system utilizing needle-free components and I.V. manifold for multiple simultaneous intravenous therapy via gravity, syringe, or infusion pump. Use of a needle-free system may aid in the prevention of needle-stick injuries.
Where Was This Sold?
This product was distributed to 19 states: AL, CA, CO, FL, IL, MI, MN, MO, MT, NV, NY, OH, OK, PA, TN, TX, UT, VA, WA
About Quest Medical, Inc.
Quest Medical, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report