Arrow recalls specific pressure injectable catheter kits due to potential sterility issues from unsealed packaging. Affected products include model ASK-15703-PVH and ASK-15703-PNYP with listed lot numbers. Consumers should check their kit's packaging for these codes.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling certain pressure injectable catheter kits because the packaging might not be sealed properly, which could lead to contamination. This is a serious risk for medical procedures where sterile equipment is essential.
The unsealed packaging could allow bacteria to enter the kit, making it unsafe for medical use. This poses a risk of infection during procedures that require sterile equipment.
Healthcare professionals and patients using these catheter kits for medical procedures. Those with the specific product codes and lot numbers listed are most at risk.
Check the product code on the packaging: ASK-15703-PVH or ASK-15703-PNYP. Look for the listed lot numbers: 13F17D0024 through 13F17L0679 for PVH and 13F17H0123 for PNYP.
Look for the product codes ASK-15703-PVH or ASK-15703-PNYP on the packaging.
Confirm the lot numbers match the listed numbers for the specific product code.
The packaging may not be sealed properly, which could lead to contamination and infection risks during medical procedures.
Check the product code and lot numbers listed in the recall notice to see if your kit is affected. If it is, contact Arrow for guidance.
The recall notice does not mention a specific fix or remedy; affected products should be checked and handled according to the recall instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1981-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1981-2018 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.
