Arrow International LLC recalls antimicrobial PSI medical kits due to potential sterility issues that could lead to serious or life-threatening injuries. Check product model numbers and batch codes for affected items.
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 International LLC is recalling antimicrobial PSI medical kits that may have sterility issues. If the sterility of the water-based injectable products is compromised, this could lead to serious or life-threatening injuries.
The supplier of the kits had quality issues, which could compromise the sterility of water-based injectable products. If the sterility is compromised, this could lead to serious or life-threatening injuries.
Medical professionals and patients who use the recalled antimicrobial PSI kits for injections or procedures. Those with the specific model numbers and batch codes listed in the recall are most at risk.
Check for model numbers like ASK-09701-UMH, ASK-09803-OSU4, and batch codes such as 10801902193275. The kits are used for medical injections and procedures.
Look for model numbers and batch codes on the product labels to determine if your kit is affected.
Reach out to Arrow International LLC for further assistance if you have the product details.
Arrow International LLC is recalling antimicrobial PSI medical kits with model numbers like ASK-09701-UMH and ASK-09803-OSU4.
Check the model number and batch code on the product label. Affected kits have model numbers listed in the recall and batch codes such as 10801902193275.
If the sterility of the water-based injectable products is compromised, this 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-2369-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2369-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
