Arrow recalls certain medical kits due to potential sterility issues in injectable products, which could lead to serious or life-threatening injuries if used.
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 specific medical kits that contain lidocaine, bupivacaine, and saline. The recall is because the supplier had quality issues that might compromise the sterility of the products, potentially causing serious or life-threatening injuries if used.
The kits contain injectable medications that could become contaminated if the sterility is compromised. This contamination might lead to serious or life-threatening infections or reactions if the products are used in medical procedures.
Healthcare professionals and patients who use these kits for medical procedures are at risk. Those who have the specific kit models listed in the recall are most affected.
Check for kit models with the following descriptions: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC, AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC, and other variants listed in the recall notice. The lot numbers and batch codes are also included in the recall.
Identify the exact model and lot number of the kit to confirm if it is recalled.
Reach out to Arrow International LLC for further assistance with the recall.
The supplier had quality issues that could compromise the sterility of the injectable products, potentially leading to serious or life-threatening injuries.
Check the model and lot number to see if it is recalled, then contact Arrow International LLC for further instructions.
If the sterility is compromised, it could lead to serious or life-threatening injuries, so it's important to verify the kit's status.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2374-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2374-2026 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.
