Arrow recalls PICC lines with Chlorag+ard Technology due to unsealed packaging potentially compromising sterility. Affected product codes include PR-44041-BAS through PR-45563-HPHNM.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling PICC lines with Chlorag+ard Technology because the packaging might not be sealed properly, which could lead to contamination. This affects specific product codes and lot numbers listed in the recall notice.
The unsealed packaging could allow contaminants to enter the PICC line, potentially causing infections. This is a sterility risk that may not cause immediate harm but requires careful handling to prevent contamination.
Patients using the recalled PICC lines for medical purposes are most at risk. The recall applies to specific product codes and lot numbers manufactured between certain dates.
Check for product codes starting with PR-44041-BAS, PR-44052-BAS, PR-44063-BAS, PR-45041-BAS, and others listed in the recall notice. Also look for specific lot numbers associated with each product code.
Identify the product code on the PICC line, which should match the codes listed in the recall notice.
Reach out to Arrow International for further assistance if you have the recalled product code.
Product codes PR-44041-BAS, PR-44052-BAS, PR-44063-BAS, PR-45041-BAS, PR-45052-BAS, PR-45063-BAS, PR-45541-BAS, PR-45541-HPHNL, PR-45541-HPHNM, PR-45552-BAS, PR-45552-HPHNL, PR-45552-HPHNM, PR-45563-BAS, PR-45563-HPHNL, and PR-45563-HPHNM are affected.
Check the product code and lot number on your PICC line against the list provided in the recall notice.
Contact Arrow International for further assistance if you have the recalled product code.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2025-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2025-2018 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.
