Arrow International LLC recalls specific catheter kits due to potential sterility issues in water-based injectable products, which could lead to serious or life-threatening injuries. Affected kits include various models with specific part numbers.
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 has recalled multiple medical catheter kits because a supplier was found to have quality issues with the lidocaine, bupivacaine, and 0.9% sodium chloride products. If the sterility of these water-based injectable products is compromised, it could lead to serious or life-threatening injuries.
The supplier of the catheter kits had quality issues with the lidocaine, bupivacaine, and 0.9% sodium chloride products. If the sterility of these water-based injectable products is compromised, it could lead to serious or life-threatening injuries.
Healthcare professionals and patients who use these catheter kits for medical procedures are most at risk. The specific kits affected include various models with detailed part numbers and batch codes.
Check for the following part numbers: ASK-42802-PLH, AK-12123-F, AK-15123-F, ASK-12703-PMAH, ASK-12703-PNM, ASK-12703-PUMH, and others listed in the recall notice. Also check the batch codes associated with these part numbers.
Review the part numbers and batch codes 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 kit is affected.
The supplier had quality issues with the lidocaine, bupivacaine, and 0.9% sodium chloride products. If sterility is compromised, it could lead to serious or life-threatening injuries.
Check for the part numbers listed in the recall notice, such as ASK-42802-PLH, AK-12123-F, and others, along with the associated batch codes.
Contact Arrow International LLC to confirm if your kit is affected and follow their instructions for next steps.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2376-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2376-2026 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.
