Arrow recalls Radial Artery Catheterization Kit model AK-04020-C with povidone iodine prep pads that expire after 24 months instead of 36. Affected kits were sold from October 2018 to March 2020.
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 certain Radial Artery Catheterization Kits because the povidone iodine prep pads don't last 36 months as required. This means the pads could become ineffective before the kit's expiration date, potentially causing infection risks during medical procedures.
The povidone iodine prep pads in some kits expire after 24 months instead of the required 36 months. This could lead to less effective disinfection during medical procedures, increasing infection risk if the pads become too old.
Healthcare professionals using the specific model kits with lots sold between October 2018 and March 2020. Patients receiving procedures with these kits may be at slightly higher risk of infection if the pads expire prematurely.
Check for the model AK-04020-C with lots numbers 13F16H0430, 13F16M0224, 13F16M0242, 13F17F0150, 13F17F0475, 13F17G0240, 23F16E1193, 23F16F0476, 23F16G0085, 23F16H0013, or 23F16H0680. These kits were sold from October 2018 through March 2020.
Look for the lot numbers listed in the recall notice to confirm if your kit is affected.
The povidone iodine prep pads in certain kits do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.
Check for the model AK-04020-C with specific lot numbers sold between October 2018 and March 2020.
The recall does not specify a remedy, so no action is required unless you want to verify the lot number.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1283-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1283-2018 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.
