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FDAJuly 14, 2023device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

quest medicalquest

UPCs

20634624952007

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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. — Recall Details · AllClear