Arrow recalls certain lots of Pressure Injectable Two-Lumen PICC Kits due to potential contamination from unsealed catheters. Affected units may not be sterile, posing infection risks during medical procedures.
Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
Arrow is recalling specific lots of Pressure Injectable Two-Lumen PICC Kits because some catheters may not be properly sealed, risking contamination during medical procedures. This could lead to infections if the kit is used without proper sterility.
The catheters may not be completely sealed, which can compromise sterility. If the kit is used without proper sterility, it could introduce infections into the patient's bloodstream during medical procedures.
Patients receiving IV treatments with the recalled kits are most at risk. Healthcare providers using the affected lots should check their inventory.
Check for the product number EU-050:052-HPMSB and lot number 13F17B0123 on the kit packaging. The recall applies to kits sold with these specific identifiers.
Look for the product number EU-05052-HPMSB and lot number 13F17B0123 on the kit packaging to confirm if it is affected.
Certain lots of the catheters may not be completely sealed, which could compromise sterility and lead to infections during medical procedures.
Check for the product number EU-05052-HPMSB and lot number 13F17B0123 on the kit packaging. If your kit has these identifiers, it is affected.
The recall does not specify a remedy, so contact Arrow International for guidance on next steps.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1325-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1325-2018 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.
