Arrow International LLC recalls multiple midline catheter kits and sets due to potential contamination with lidocaine, bupivacaine, and 0.9% sodium chloride. The supplier had quality issues that could lead to serious or life-threatening injuries if sterility is compromised.
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 several midline catheter kits and sets because the supplier had quality issues with the drugs inside. If the sterility of the water-based injectable products is compromised, this could lead to serious or life-threatening injuries.
The supplier had quality issues with the drugs (lidocaine, bupivacaine, and 0.9% sodium chloride) in the kits. If the sterility of the water-based injectable products is compromised, this could lead to serious or life-threatening injuries.
Healthcare professionals who use these catheter kits for medical procedures are most at risk. Patients receiving these kits as part of their treatment may also be affected.
Check for the product codes listed in the recall: CDC-02031-MK1A, CDC-41541-MPK1A, CDC-41552-MPK1A, and other specific model numbers and batch codes provided in the recall notice.
Review the product codes and batch numbers listed in the recall notice to confirm if your catheter kit is affected.
Reach out to Arrow International LLC for further assistance or to confirm if your specific model is recalled.
The recall includes midline catheter kits and sets with specific model numbers and batch codes listed in the notice, such as CDC-02031-MK1A, CDC-41541-MPK1A, CDC-41552-MPK1A, and others.
The supplier had quality issues with the drugs (lidocaine, bupivacaine, and 0.9% sodium chloride) in the kits, which could lead to serious or life-threatening injuries if the sterility of the water-based injectable products is compromised.
Check the product codes and batch numbers listed in the recall notice to confirm if your catheter kit is affected. Contact Arrow International LLC for further assistance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2394-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2394-2026 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.
