Arrow recalls Two-Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter due to incorrect priming volume labeling on the lidstock. This may cause errors in medical procedures.
The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct
Arrow is recalling a specific catheter kit because the lidstock has a labeling error showing the wrong priming volume. This could lead to medical errors during procedures if healthcare workers use the kit without noticing the mistake.
The lidstock incorrectly states the priming volume, which is the amount of fluid needed to prepare the catheter. This error could cause healthcare workers to use the wrong volume during procedures, potentially leading to medical errors.
Healthcare professionals using the specific model of catheter kit with the listed lot numbers are affected. Patients receiving care from these kits may be at risk of procedural errors.
Check for the product code AH-11802 (OUS) and lot numbers listed in the recall notice. The kit includes a blue FlexTip catheter and is used for central venous catheterization.
Verify the product code and lot numbers to confirm if your kit is affected.
The recall is for a labeling error that could lead to medical errors if the wrong priming volume is used, but it does not pose an immediate risk to users.
Check the product code and lot numbers to see if your kit is affected; if it is, contact Arrow for further instructions.
Look for the product code AH-11802 (OUS) and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1118-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1118-2019 from Arrow. 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.
