Arrow recalls spinal anesthesia kits with potential sterility issues that could cause serious or life-threatening injuries. Affected kits include specific models and batch numbers. Consumers should contact Arrow for details.
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 certain spinal anesthesia kits due to quality issues with the drugs inside, which could lead to serious or life-threatening injuries if the sterility is compromised. These kits are used for medical procedures and should be checked for the specific model numbers and batch codes listed.
The kits contain lidocaine, bupivacaine, and saline solution that may have been contaminated, compromising sterility. If the drugs are not sterile, they could cause serious or life-threatening injuries during medical procedures.
Medical professionals who use these spinal anesthesia kits for procedures are most at risk. Patients receiving these kits during surgery could be affected if the drugs are contaminated.
Check for model numbers like ASA-24090-SB, ASA-24103-SB, or ASK-24090-SA on the kit. Also look for batch numbers such as 10801902193275 or 33F24G0383 on the packaging.
Look for model numbers and batch codes on the kit packaging to confirm if it is affected.
Reach out to Arrow International LLC for specific instructions on what to do with the affected kits.
The supplier had quality issues with the drugs in the kits, which could lead to contamination and serious or life-threatening injuries if sterility is compromised.
Affected models include ASA-24090-SB, ASA-24103-SB, ASK-24090-SA, and others with specific batch numbers listed in the recall notice.
No, but you should check the model and batch numbers to see if your kit is affected. Contact Arrow for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2389-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2389-2026 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.
