Arrow recalls specific CVC kits due to potential contamination of lidocaine, bupivacaine, and saline. If the product is not sterile, it could cause serious or life-threatening injuries.
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 certain central venous catheter (CVC) kits because they may contain contaminated medication. Using these kits could lead to serious or life-threatening infections if the medication is not sterile.
The supplier had quality issues that could compromise the sterility of the medication. If the medication is not sterile, it might cause serious infections or life-threatening reactions in patients.
Healthcare professionals who use these CVC kits for medical procedures are most at risk. Patients receiving treatment with these kits could face serious infections.
Check for the model numbers: ASK-42703-PNHS2, ASK-45703-PNHS2, or ASK-45854-PNHS2. These kits were sold with specific batch numbers and lot codes.
Discard any CVC kits with the model numbers ASK-42703-PNHS2, ASK-45703-PNHS2, or ASK-45854-PNHS2.
The supplier had quality issues that could compromise the sterility of the medication, potentially leading to serious or life-threatening injuries.
Discard the kits immediately and contact Arrow for replacement if needed.
Yes, if the medication is not sterile, it could cause serious infections or life-threatening reactions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2375-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2375-2026 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.
