Arrow recalls multiple hemodialysis kits due to potential sterility issues with lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if not properly sterilized.
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Arrow is recalling several hemodialysis kits that contain lidocaine, bupivacaine, and saline solutions. The supplier had quality issues that could compromise the sterility of these products, leading to serious or life-threatening injuries if used.
The supplier had quality issues that could compromise the sterility of the water-based injectable products. If the sterility is compromised, it could lead to serious or life-threatening injuries due to contamination.
Healthcare professionals and patients using hemodialysis treatments who own the recalled kits are affected. Those with the specific model numbers listed in the recall are at the highest risk.
Check the product model numbers listed in the recall, such as AK-11802-F, AK-22122, AK-22142-CDC, and others. Also, look for the batch numbers like 10801902193275 or 33F24G0344.
Identify the model number on the kit, such as AK-11802-F, AK-22122, or AK-22142-CDC.
Reach out to Arrow International LLC for further instructions on the recall.
The supplier had quality issues that could compromise the sterility of the water-based injectable products, which could lead to serious or life-threatening injuries if not properly sterilized.
Check the model number and batch number on the kit. Contact Arrow International LLC for further instructions.
The recall states that if sterility is compromised, it could lead to serious or life-threatening injuries, but the risk is not immediate unless the product is not properly sterilized.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2373-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2373-2026 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.
