Arrow International LLC recalls hemodialysis kits that may contain contaminated solutions. If sterility is compromised, serious or life-threatening injuries could occur. Check product codes and batch numbers listed in the recall notice.
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 International LLC is recalling certain hemodialysis kits due to potential contamination in the solutions. If the sterility of the water-based injectable products is compromised, this could lead to serious or life-threatening injuries.
The supplier of the kits had quality issues, which could lead to contamination of the water-based injectable products. If sterility is compromised, this could cause serious or life-threatening injuries.
People using hemodialysis kits with the specific model numbers and batch numbers listed in the recall notice. Patients on dialysis who use these kits are at risk.
Check for model numbers and batch numbers listed in the recall notice. The kits include specific product codes like AK-15122-F, ASK-12123-UOC1, and CDC-12123-P1A with associated batch numbers.
Look for model numbers and batch numbers on the kit packaging to confirm if it is recalled.
Arrow International LLC is recalling certain hemodialysis kits that may contain contaminated solutions due to supplier quality issues.
If the sterility of the water-based injectable products is compromised, this could lead to serious or life-threatening injuries.
Check the model numbers and batch numbers listed in the recall notice, such as AK-15122-F, ASK-12123-UOC1, and CDC-12123-P1A with associated batch numbers.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2388-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2388-2026 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.
