Arrow recalls HemoDialysis Kits with CDC-25142-X1A lot numbers due to potential contamination. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits include specific batch numbers.
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 HemoDialysis Kits that may contain contaminated drugs. If the sterility of the water-based injectable products is compromised, this could lead to serious or life-threatening injuries.
The supplier had quality issues with the drugs, including lidocaine, bupivacaine, and 0.9% sodium chloride. If the sterility of the water-based injectable product is compromised, it could cause serious or life-threatening injuries.
Healthcare professionals and patients using the recalled HemoDialysis Kits are at risk. Those who have the specific batch numbers listed in the recall are most vulnerable.
Check the kit's batch number on the label, which should be CDC-25142-X1A. The affected kits include specific batch numbers: 30801902123597, 10801902193275, and 33F25B0467.
Immediately stop using the recalled HemoDialysis Kit if you have the specific batch numbers listed in the recall.
The affected batch numbers are 30801902123597, 10801902193275, and 33F25B0467.
The supplier had quality issues with the drugs, which could lead to serious or life-threatening injuries if the sterility of the water-based injectable product is compromised.
Immediately stop using the kit and 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-2372-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2372-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
