Arrow recalls Blue PLUS Pressure Injectable Multi-Lumen CVC Kits with unsealed packaging that may compromise sterility. Affected units include specific product codes and lot numbers. Consumers should check their kit details and contact Arrow for guidance.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling certain Blue PLUS Pressure Injectable Multi-Lumen CVC Kits because the packaging might not be sealed properly, which could lead to contamination. This risk affects medical devices used for intravenous access, so it's important to stop using the recalled kits to prevent infection.
The unsealed packaging could allow contaminants to enter the kit, potentially compromising sterility. This risk is specific to medical devices used for intravenous access, where contamination could lead to infections if the kit is used without proper sterilization.
Healthcare professionals and patients using the recalled Arrow Blue PLUS Pressure Injectable Multi-Lumen CVC Kits are most at risk. The specific product codes and lot numbers listed in the recall affect medical devices used for intravenous access.
Check for product codes CDC-45703-P1A, CDC-45703-PB1A, CDC-42703-P1A, or CDC-15703-P1A on the packaging. The recall includes specific lot numbers listed in the official notice.
Look for the product codes CDC-45703-P1A, CDC-45703-PB1A, CDC-42703-P1A, or CDC-15703-P1A on the kit packaging.
Reach out to Arrow International Inc. for further guidance on the recall and next steps.
The recall is due to unsealed packaging that may compromise sterility, which could lead to contamination if the kit is used without proper sterilization.
Product codes CDC-45703-P1A, CDC-45703-PB1A, CDC-42703-P1A, and CDC-15703-P1A are affected, along with specific lot numbers listed in the recall notice.
The recall does not require immediate discontinuation; however, you should check if your kit is affected and contact Arrow 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-1994-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1994-2018 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.
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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.
