Arrow recalls Blue PLUS Multi-Lumen CVC kits with unsealed packaging that may compromise sterility. Affected units include specific lot numbers. Consumers should check product details and contact Arrow for guidance.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Blue PLUS Multi-Lumen CVC kits with Blue FlexTip catheters due to potential unsealed packaging that could compromise sterility. This risk affects medical devices used in patient care, so proper sterilization is critical to prevent infections.
The packaging may not be sealed properly, which could allow contamination. This poses a risk of infection if the sterile medical device is used without proper sterilization.
Healthcare professionals and patients using the Arrow Blue PLUS Multi-Lumen CVC kits with Blue FlexTip catheters. Those with the specific lot numbers listed in the recall are most at risk.
Check for the product code MSO-45703-AHS and lot numbers 13F17C0230, 13F17D0161, 13F17F0068, 13F17G0364, 13F17H0351, 13F17J0387, 13F17K0579, or 13F17L0487.
Verify the product code MSO-45703-AHS and lot numbers listed in the recall to confirm if your item is affected.
The packaging may not be sealed properly, which could compromise sterility and lead to infection risks.
Check the product code and lot numbers to see if it's affected. If it is, contact Arrow for guidance.
The recall does not specify a fix; affected units should be checked and contacted for guidance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2018-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2018-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
