Arrow International recalls Blue PLUS Triple-Lumen CVC Kits with unsealed packaging that may compromise sterility. Affected units include specific lot numbers. Consumers should check their product details and contact Arrow for guidance.
Product sterility may be compromised due to unsealed packaging.
Arrow International is recalling Blue PLUS Triple-Lumen CVC Kits with Blue FlexTip Catheters due to unsealed packaging that could compromise sterility. This means the medical devices might become contaminated, posing a risk during medical procedures.
The packaging may not be properly sealed, which could allow contamination of the sterile medical device. If the device is used without proper sterility, it might lead to infections or other complications during medical procedures.
Healthcare professionals and patients using the ARROWgard Blue PLUS Triple-Lumen CVC Kit with Blue FlexTip Catheter. Those with the specific lot numbers listed in the recall are most at risk.
Check for the product code ASK-45703-VC and lot numbers 13F17A0219, 13F17C0013, 13F17C0431, 13F17D0166, 13F17F0070, 13F17F0714, 13F17G0590, or 13F17J0392, 13F17L0070 on the packaging.
Look for the product code ASK-45703-VC and the listed lot numbers on the packaging to confirm if your item is affected.
The packaging may not be properly sealed, which could lead to contamination of the sterile medical device.
Check the product code and lot numbers on the packaging to see if it's affected. If it is, contact Arrow International for guidance.
The recall does not specify a fix; affected units should be checked and contacted for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2005-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2005-2018 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.
