Arrow International LLC recalls specific PSI kits due to potential sterility issues in water-based injectables, which could cause serious or life-threatening injuries. Affected kits have model numbers starting with ASK or CDC prefixes.
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 is recalling several PSI medical kits because they may contain water-based injectables with compromised sterility. If the sterility is broken, this could lead to serious or life-threatening infections or injuries.
The kits contain lidocaine, bupivacaine, and saline solutions that are water-based. If the sterility of these injectables is compromised, it could lead to serious or life-threatening infections or injuries.
Medical professionals who use these kits for injections or procedures are most at risk. Patients receiving injections from these kits could also be affected if the sterility is compromised.
Check for model numbers starting with ASK or CDC prefixes like ASK-09701-UP, ASK-09803-OSU5, or CDC-09903-1A. These kits were sold with specific batch numbers listed in the recall notice.
Identify the model number on the kit, which starts with ASK or CDC prefixes like ASK-09701-UP or CDC-09903-1A.
Reach out to Arrow International LLC for guidance on whether your kit is affected and what to do next.
The supplier had quality issues with the water-based injectables, which could lead to compromised sterility and serious or life-threatening injuries.
PSI kits with model numbers starting with ASK or CDC prefixes, such as ASK-09701-UP, ASK-09803-OSU5, or CDC-09903-1A, as listed in the recall notice.
The recall does not require immediate discontinuation; medical professionals should check the model number and contact Arrow International LLC for guidance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2393-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2393-2026 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.
