Arrow recalls several medical kits due to potential contamination of sterile products, which 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 is recalling multiple medical kits that contain lidocaine, bupivacaine, and saline solutions. The supplier had quality issues that could compromise sterility, risking serious or life-threatening injuries if the products are used.
The supplier had quality issues that could compromise the sterility of water-based injectable products. If the products are not sterile, they could cause serious or life-threatening infections or reactions when injected.
Healthcare professionals and patients using these kits for procedures like epidural anesthesia or nerve blocks are at risk. The most vulnerable are those who have already used the recalled kits.
Check for the product names and model numbers listed in the recall notice. The kits include specific names like 'STIMUCATH SFTY KIT' and model codes such as 'ASK-04001-SUH-S' or 'AB-19604-KS'.
Identify the specific kit and model numbers listed in the recall notice to confirm if your product is affected.
The supplier had quality issues that could compromise sterility of the products, which may lead to serious or life-threatening injuries if the products are not sterile.
The official recall notice does not specify a remedy or action steps for affected products.
Yes, if the sterility of the products is compromised, it could lead to serious or life-threatening injuries.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2364-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2364-2026 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.
