Arrow recalls certain Pacing PSI kits due to potential contamination in lidocaine, bupivacaine, and saline solutions. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits have specific batch numbers.
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 specific Pacing PSI kits that may contain contaminated lidocaine, bupivac: 0.9% sodium chloride. If the sterility of the injectable solution is compromised, it could cause serious or life-threatening injuries.
The supplier had quality issues with the drugs, which could lead to contamination. If the injectable solution is not sterile, it might cause infections or other serious health problems during medical procedures.
Healthcare professionals using the recalled kits for medical procedures are most at risk. Patients receiving treatments with these kits could face serious or life-threatening complications.
Check for the batch number 10801902210217 on the kit's label. The product was sold with the reference code ASK-07155-MGU.
Immediately stop using the recalled Pacing PSI kit if you have it.
The supplier had quality issues with the drugs, which could lead to contamination. If the injectable solution is not sterile, it might cause serious or life-threatening injuries.
The affected batch number is 10801902210217.
Check the batch number on the kit's label; the affected batch is 10801902210217.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2383-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2383-2026 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.
