Reported Nov 8, 2023 · Ongoing
Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets…
Quest Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Quest Medical, Inc. · 1 Allentown Pkwy · Allen, TX · 75002-4206
Is this the product you have?
- Q2 Multiport Extension set
- REF9520, 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
- Lot codes and dates
- Lots
6908369136693296933069396693976947169472
- UDI(01)20634624952007
- Lots
- Amount recalled
- 17,700 units
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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