Arrow recalls ErgoPack PICC kits with incorrect labeling on lidstock. Affected kits have a specific batch number and may need verification to avoid confusion.
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Arrow is recalling certain ErgoPack PICC kits because the product name and code were listed incorrectly on the lidstock. This labeling error could lead to confusion about which kits are being used.
The kits have incorrect product names and codes on the lidstock. This labeling error could cause healthcare providers to use the wrong kit, potentially leading to incorrect medical procedures.
Healthcare professionals using Arrow ErgoPack PICC kits with batch number 13F22E0359 are likely affected. Patients receiving these kits may be at risk if the incorrect labeling causes confusion.
Check for the batch number 13F22E0359 on the lidstock of the Arrow ErgoPack PICC kit. The product is a pressure injectable two-lumen PICC catheter pre-loaded with Arrow VPS Stylet.
Check the lidstock for the correct product name and code to ensure it matches the batch number 13F22E0359.
The recall is due to incorrect product names and codes listed on the lidstock of affected kits.
Batch number 13F22E0359.
No, but you should verify the labeling to ensure you are using the correct kit.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2591-2023 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2591-2023 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.
