ARROW recalls a specific midline IV kit due to mislabeled catheter size. This could lead to incorrect use if the wrong catheter is used. Affected units have a specific product code and reference number.
Mislabeling: the corrugate label, lidstock, banner card, and peel sticker accompanying the affected product incorrectly displays a double lumen 5.5 French catheter (and related priming volumes and kit contents for product code ASK-41552-JHVA1), instead of the packaged single-lumen 4.5 French catheter (and related priming volumes and kit contents for product code ASK-41541-JHVA1).
ARROW is recalling a specific midline IV kit because it's mislabeled as a two-lumen catheter instead of a single-lumen one. Using the wrong catheter could cause incorrect medical procedures or complications.
The kit is labeled as a two-lumen catheter but contains a single-lumen catheter. This mismatch could lead to incorrect medical procedures if the wrong cath: 1. The kit is intended for intravenous therapy, blood sampling, and pressure injection of contrast media. 2. Using the wrong catheter size could cause complications like incorrect fluid flow rates or improper connections.
Healthcare professionals using this specific IV kit for medical procedures are most at risk. Patients receiving treatment with the affected kit could experience complications if the wrong catheter is used.
Check for the product code ASK-41552-JHVA1 on the label or packaging. The kit includes a specific catheter size (5.5 Fr, 15 cm) and is part of the Arrowg+ard Blue Advance series.
Look for the product code ASK-41552-JHVA1 on the label or packaging to confirm if the kit is affected.
The kit is mislabeled and could lead to incorrect use if the wrong catheter is used. Do not use the affected kit without verifying the product code.
The affected kit has the product code ASK-41552-JHVA1.
Check the label or packaging for the product code ASK-41552-JHVA1 and the specific catheter size (5.5 Fr, 15 cm).
We’ve drafted a message you can send ARROW to request your refund or repair — edit it as you like.
Subject: Recall Z-0102-2023 — ARROW ARROW Hello, I own a ARROW that is covered by recall Z-0102-2023 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.
