Arrow recalls Radial Arterial Access Kit (ASK-04001-BID2) due to potential sterility compromise from unsealed packaging. Affected units include specific lot numbers.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling a Radial Arterial Access Kit because its packaging might not be sealed properly, which could lead to contamination. This is a serious risk for medical procedures requiring sterile conditions.
The unsealed packaging could allow contaminants to enter the kit, risking infection during medical procedures. This is especially dangerous for critical surgeries or procedures where sterility is essential.
Healthcare professionals using this kit for medical procedures are most at risk. Patients receiving the kit could face infection if the packaging is compromised.
Check for the product code ASK-04001-BID2 on the kit. Affected units include lot numbers 13F17A0195, 13F17D0213, 13F17F0428, 13F17K0314, and 13F17L0113.
Immediately stop using the recalled Radial Arterial Access Kit if it has the listed lot numbers.
The packaging may not be sealed properly, which could lead to contamination during medical procedures.
Lot numbers 13F17A0195, 13F17D0213, 13F17F0428, 13F17K0314, and 13F17L0113.
The recall does not provide a fix; users must stop using the kit immediately.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1968-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1968-2018 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.
