Arrow recalls Access Tray model ASK-04001-MC3 due to potential contamination of lidocaine and bupivacaine in medication kits, which could cause 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 Access Tray model ASK-04001-MC3 because medication kits it supplied may have been contaminated, risking serious or life-threatening injuries if the sterility of the injectable products is compromised.
The supplier of the medication kits used in the Access Tray 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 injuries when injected.
Healthcare professionals using the Access Tray model ASK-04001-MC3 for medication administration are most at risk if the medication kits contain contaminated products.
Check for the model number ASK-04001-MC3 on the Access Tray. The product was sold with the reference code ASK-04001-MC3.
Immediately stop using the Access Tray model ASK-04001-MC3 if it is used for medication administration, as contaminated products could cause serious or life-threatening injuries.
The supplier of the medication kits used in the Access Tray had quality issues that could compromise the sterility of water-based injectable products, potentially leading to serious or life-threatening injuries.
Immediately stop using the Access Tray model ASK-04001-MC3 if it is used for medication administration, as contaminated products could cause serious or life-threatening injuries.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2392-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2392-2026 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.
