Arrow recalls Central Venous Catheter Kits 16/18 gauge multi-lumen models CDC-45703-XP1A (IPN035619, IPN036437, IPN922677) sold between June 1-September 30, 2021 due to potential temperature exposure affecting product effectiveness.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Arrow is recalling certain central venous catheter kits that were sold between June and September 2021. These kits may have been exposed to higher temperatures during shipping, which could reduce their effectiveness. This recall affects healthcare facilities that used these specific kits.
The kits were shipped between June 1 and September 30, 2021, and may have experienced temperature fluctuations during transit. Exposure to higher temperatures could reduce the product's effectiveness, but it does not pose an immediate risk of injury or death.
Healthcare facilities that purchased the recalled catheter kits between June 1 and September 30, 2021. Staff using these kits for medical procedures are most at risk if the kits were exposed to higher temperatures.
Check for model number CDC-45703-XP1A with IPN numbers 035619, 036437, or 922677. These kits were sold between June 1 and September 30, 2021, by Arrow.
Verify the model number and IPN codes on the kit packaging to confirm if it is part of the recall.
The kits may have been exposed to higher temperatures during shipping from June 1 to September 30, 2021, which could reduce their effectiveness.
No, the recall does not require immediate discontinuation. The kits may still be used but their effectiveness could be reduced.
Check the product details to confirm if you have the recalled kits. If you do, contact Arrow for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1604-2022 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1604-2022 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.
