Arrow recalls peritoneal lavage catheter kits with lot numbers AK-09000/30801902121722 and others due to potential sterility issues that could cause serious infections.
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 peritoneal lavage catheter kits that may have sterility problems. If the kits are contaminated, they could cause serious infections or life-threatening complications during medical procedures.
The kits may contain contaminated solutions due to supplier quality issues. If the sterile water-based injectable products are compromised, they could lead to serious infections or life-threatening complications during medical procedures.
Patients using peritoneal lavage catheter kits from Arrow with specific lot numbers are affected. Healthcare providers and patients undergoing peritoneal dialysis are at highest risk.
Check the lot numbers on the kit packaging: AK-09000/30801902121722, 10801902193275, 20801902121756, and others listed in the recall notice.
Look for lot numbers on the kit packaging: AK-09000/30801902121722, 10801902193275, 20801902121756, and other specific numbers listed in the recall.
The supplier had quality issues that could compromise the sterility of the water-based injectable products, potentially leading to serious infections.
Check the lot numbers on the kit packaging. If it matches the listed numbers, contact Arrow for instructions on how to handle it.
Yes, if the sterility is compromised, it could lead to serious infections or life-threatening complications during medical procedures.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2380-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2380-2026 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.
