Arrow recalls arterial line kits that may contain contaminated medication, risking serious injury or death. Affected kits include specific models and batch numbers. Consumers should stop using and contact Arrow for details.
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 arterial line kits that may contain contaminated medication due to supplier quality issues. If the sterility of the medication is compromised, it could lead to serious or life-threatening injuries.
The supplier had quality issues with the medication, which could compromise the sterility of the water-based injectable products. If the medication is not sterile, it could cause serious or life-threatening injuries when used in medical procedures.
Medical professionals who use these arterial line kits for procedures like blood draws or IV access are most at risk. The kits are used in hospitals and clinics.
Check the product model numbers and batch numbers listed in the recall notice. Affected kits include specific models like SL 20 GA X 5 IN/ASK-04510-MM6 and batch numbers such as 10801902193275.
If you have any of the affected arterial line kits, stop using them right away to prevent potential serious injury.
The supplier had quality issues with the medication, which could compromise the sterility of the water-based injectable products, leading to serious or life-threatening injuries.
Affected kits include specific models like SL 20 GA X 5 IN/ASK-04510-MM6 and batch numbers such as 10801902193275.
Check the product model numbers and batch numbers listed in the recall notice. Affected kits include specific models like SL 20 GA X 5 IN/ASK-04510-MM6 and batch numbers such as 10801902193275.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2377-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2377-2026 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.
