Angiodynamics recalls fluid management kits with specific lot numbers due to assembly issues causing minor procedure delays. Affected kits may not function properly during medical procedures.
NAMIC Fluid Management Convenience Kits contains a Fluid Delivery Set that was not assembled in accordance with specification, and prevents the device from being used, resulting in a minor delay in procedure.
Angi:odynamics recalls certain fluid management kits used in medical procedures because they were not assembled correctly, which can cause minor delays during surgery. This does not pose a serious safety risk but requires immediate attention to avoid procedure delays.
The kits contain a Fluid Delivery Set that was not assembled properly, which prevents the device from functioning correctly. This issue causes minor delays in medical procedures but does not involve physical harm or serious injury.
Medical professionals using the recalled kits for fluid management or invasive pressure monitoring procedures are affected. Patients undergoing these procedures may experience minor delays due to the faulty kits.
Check the lot numbers on the kit: 5284422, 5286610, 5283649, 5290525, or 5286542. These kits were sold for use in fluid management and invasive pressure monitoring systems.
Identify the lot numbers on the kit: 5284422, 5286610, 5283649, 5290525, or 5286542.
The Fluid Delivery Set in these kits was not assembled correctly, causing minor delays in medical procedures.
Check the lot numbers to see if your kit is affected. If it is, contact the manufacturer for further instructions.
No, the recall only addresses minor procedure delays and does not involve serious injury risks.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1390-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1390-2018 from Angiodynamics. 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.
