Quest Medical recalls Q2 Multiport Extension sets (REF: 9520) due to potential needle-stick injury risk during IV fluid administration. Affected units include specific lots and UDI numbers.
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.
Quest Medical is recalling Q2 Multiport Extension sets (REF: 9520) because they may cause needle-stick injuries during IV fluid administration. This risk is particularly concerning for healthcare workers handling the sets.
These sets include needle-free components designed to prevent needle-stick injuries during IV therapy. However, the recall indicates a potential risk that could lead to needle-stick injuries despite the intended safety features.
Healthcare professionals who use these IV sets for patient care are most at risk. Patients receiving IV therapy using these sets could also be affected.
Check for the product name 'Q2 Multiport Extension set' with reference number 9520. Affected units include specific lots: 69083, 69136, 69329, 69330, 69396, 69397, 69471, 69472, and UDI number (01)20634624952007.
Identify the product by checking the reference number (9520) and lot numbers listed in the recall notice.
The recall is due to a potential risk of needle-stick injuries during IV fluid administration, even though the sets are designed to prevent such injuries.
Affected lots include 69083, 69136, 69329, 69330, 69396, 69397, 69471, and 69472.
Check for the reference number 9520 and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Quest Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0197-2024 — Quest Medical Quest Medical Hello, I own a Quest Medical that is covered by recall Z-0197-2024 from Quest Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
