Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send ConMed Corporation to request your refund or repair — edit it as you like.
Subject: Recall Z-0805-2018 — ConMed Corporation ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Needle-Free Controller Prim Hello, I own a ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) that is covered by recall Z-0805-2018 from ConMed Corporation. 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.
