Arrow recalls Radial Artery Catheterization Kit model AK-04020 with povidone iodine prep pads that expire after 24 months instead of 36. These pads may not be safe for long-term use.
The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
Arrow is recalling Radial Artery Catheterization Kit model AK-04020 because the povidone iodine prep pads don't meet 36-month shelf life requirements and should be labeled for 24 months. This means the pads could become unsafe over time if not used within their shorter expiration period.
The povidone iodine prep pads in certain kits do not meet the required 36-month shelf life. Instead, they should have a 24-month shelf life label. If these pads expire before being used, they may not be effective for disinfection, potentially increasing infection risk during medical procedures.
Healthcare professionals using the Radial Artery Catheterization Kit model AK-04020 with povidone iodine prep pads manufactured between October 2018 and March 2020 are affected. Patients receiving care from these kits may be at risk if the pads expire.
Check for the model AK-04020 on the kit. The povidone iodine prep pads were manufactured with expiration dates from October 2018 through March 2020. The pads should have a 24-month shelf life label instead of 36 months.
Look for the expiration date on the povidone iodine prep pads, which should be between October 2018 and March 2020.
The povidone iodine prep pads in certain kits do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
Check for the model AK-04020 on the kit with expiration dates from October 2018 through March 2020.
No, but you should check the expiration date on the povidone iodine prep pads to ensure they are within the 24-month shelf life period.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1282-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1282-2018 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.
