Arrow recalls PICC access trays with specific lot numbers due to potential contamination of lidocaine and bupivacaine. This could lead to serious or life-threatening injuries if the medication is not sterile.
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 PICC access trays with certain lot numbers because the medication inside may not be sterile. This could cause serious or life-threatening injuries if the medication is contaminated.
The medication in the trays (lidocaine, bupivacaine, and saline) may have been contaminated, compromising sterility. If the medication is not sterile, it could lead to serious or life-threatening infections or injuries.
Healthcare professionals who use these PICC access trays for administering medication are most at risk. Patients receiving medication through these trays could also be affected.
Check the lot numbers on the tray: 10801902193275, 33F25C0224, 33F25D0647, 33F25G0390, or 33F25J0348. These are specific to the recalled product.
Immediately stop using the PICC access tray if it has the listed lot numbers as it may contain contaminated medication.
The supplier had quality issues with the medication, which could lead to contamination and serious or life-threatening injuries if the medication is not sterile.
The affected lot numbers are 10801902193275, 33F25C0224, 33F25D0647, 33F25G0390, and 33F25J0348.
Check the lot numbers on the tray; if they match the listed numbers, it is part of this recall.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2395-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2395-2026 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.
