Arrow recalls radial artery catheterization kits with sharps safety features due to potential sterility compromise from unsealed packaging. Affected product codes include ASK-04020-RIHM and specific lot numbers.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling radial artery catheterization kits with sharps safety features because the packaging might not be sealed properly, which could lead to contamination. This is a safety issue for medical professionals using the kits.
The unsealed packaging could allow contamination of the catheter components, potentially leading to infections or other complications during medical procedures. This is a sterility risk that could compromise the safety of the procedure.
Medical professionals who use these catheter kits during procedures are most at risk. Patients using the kits are not directly affected by this recall.
Check for product codes starting with ASK-04020-RIHM. Lot numbers 13F17C0179, 13F17E0655, 13F17G0301, 13F17H0284, 13F17K0566, and 13F17M0019 are affected.
Verify the product code is ASK-04020-RIHM to determine if it is affected.
No, patients are not directly affected by this recall. The risk is for medical professionals using the kits during procedures.
The recall does not specify a remedy, so check the product code and lot numbers to see if it is affected. If affected, contact Arrow for further instructions.
Look for product code ASK-04020-RIHM and lot numbers 13F17C0179, 13F17E0655, 13F17G0301, 13F17H0284, 13F17K0566, or 13F17M0019.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1972-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1972-2018 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.