Arrow recalls specific pressure injectable catheter kits due to potential sterility issues from unsealed packaging. Affected units include model ASK-45703 with certain lot numbers. Consumers should check their product codes and lot numbers for recall.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling pressure injectable multi-lumen catheter kits that may have unsealed packaging, risking sterility. This could lead to infections if the kit is used without proper sterility. Affected units have specific product codes and lot numbers listed in the recall.
The packaging may not be sealed properly, which could allow contamination. If the kit is used without proper sterility, it might lead to infections in patients or healthcare workers.
Healthcare professionals using the catheter kits for medical procedures are most at risk. Patients receiving these kits may also be affected if the sterility is compromised.
Check for product codes ASK-45703-LDP1, ASK-45703-PBHS, or ASK-45703-PHMC. Look for specific lot numbers listed in the recall notice.
Identify your catheter kit's product code from the list: ASK-45703-LDP1, ASK-45703-PBHS, or ASK-45703-PHMC.
Compare your lot numbers with those listed in the recall notice to determine if your kit is affected.
The recall is for potential sterility issues due to unsealed packaging, which could lead to infections if the kit is used without proper sterility. However, the risk is low if the packaging is intact.
Check your product code against ASK-45703-LDP1, ASK-45703-PBHS, or ASK-45703-PHMC and verify your lot number against the list provided in the recall notice.
The recall does not specify a remedy, so you should contact Arrow directly 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-1995-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1995-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
