Arrow recalls biopsy system kits with potential contamination in lidocaine, bupivacaine, or saline solutions that could cause serious injury or illness.
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 biopsy system kits that may contain contaminated lidocaine, bupivacaine, or saline solutions. Using these kits could lead to serious injury or illness if the drugs are not sterile.
The supplier had quality issues with the drugs, which could compromise sterility. If the drugs are not sterile, they might cause serious or life-threatening injuries when injected.
Patients who use these biopsy kits for medical procedures are at risk. Healthcare providers using the kits for procedures are most vulnerable.
Check for the model numbers ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, or ASK-09458-VU on the kit. These kits were sold with specific batch numbers listed in the recall notice.
Identify the model number on the kit to see if it matches the recalled models: ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, or ASK-09458-VU.
Reach out to Arrow International LLC for guidance on next steps if you have a recalled kit.
The kits contain lidocaine, bupivacaine, and 0.9% sodium chloride.
The supplier had quality issues that could compromise the sterility of the drugs, potentially leading to serious or life-threatening injuries.
Check the model number on the kit. Recalled models include ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, or ASK-09458-VU with specific batch numbers listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2365-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2365-2026 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.
