Arrow recalls ErgoPack kits with incorrect labeling on lids. Affected kits have a specific batch number and may need replacement due to mislabeled product codes.
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 kits because the product code and name were incorrectly listed on the lidstock. This labeling error could lead to confusion about which kit is being used, potentially causing incorrect medical procedures.
The kits have incorrect product codes and names printed on the lidstock. This labeling error means healthcare workers might use the wrong kit for procedures, which could lead to incorrect medical treatments.
Healthcare professionals using Arrow ErgoPack kits with the batch number 33F23B0781 are likely affected. Those who use these kits for medical procedures may be at risk of using the wrong product due to mislabeling.
Check for the batch number 33F23B0781 on the kit's lidstock. The affected kits are labeled as Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet.
Look for the batch number 33F23B0781 on the lidstock of the kit.
The product code and name were incorrectly listed on the lidstock of affected kits, which could lead to confusion about which kit is being used.
Check the batch number on the lidstock. If it's 33F23B0781, contact Arrow for guidance.
The recall is due to labeling errors, not a safety hazard. There is no risk of serious injury from the product itself.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0001-2024 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0001-2024 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.
