Arrow recalls Radial Artery Catheterization Kit (AK-04122) 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 Radial Artery Catheterization Kits (model AK-04122) because the povidone iodine prep pads have a 24-month shelf life instead of the required 36 months. This means the pads could become ineffective or unsafe over time, potentially leading to improper medical procedures.
The povidone iodine prep pads in these kits expire after 24 months instead of the required 36 months. This could mean the pads become less effective over time, potentially leading to improper disinfection of the skin before procedures. However, the hazard is not immediate or life-threatening under normal use conditions.
Healthcare professionals using the specific model kits (AK-04122) sold between October 2018 and March 2020 are most at risk if they rely on these pads for procedures. Patients using these kits are generally not affected directly.
Check for the model number AK-04122 on the kit. The kits were sold with expiration dates from October 2018 through March 2020. Look for the lot numbers 13F16H0329, 13F17F0074, or 13F17G0237.
Verify the expiration date on the kit packaging; affected kits expire after 24 months instead of 36 months.
The povidone iodine prep pads in these kits do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.
Look for the model number AK-04122 on the kit, with lot numbers 13F16H0329, 13F17F0074, or 13F17G0237, and expiration dates from October 2018 through March 2020.
No, the recall does not require stopping use; it only addresses the shelf life of the prep pads. Proper use with current expiration dates is safe.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1285-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1285-2018 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.
