Arrow recalls specific Pacing PSI kits due to potential sterility issues with lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if not properly sterilized.
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 Pacing PSI kits because the supplier had quality issues that might compromise the sterility of the medication. This could lead to serious or life-threatening injuries if the solution is not sterile.
The supplier had quality issues that could compromise the sterility of the medication. If the solution is not sterile, it could lead to serious or life-threatening infections or injuries during medical procedures.
Patients using the recalled Pacing PSI kits for medical procedures are at risk. Healthcare providers who use these kits for injections may need to take extra care to avoid infection.
Check the product label for the model numbers: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, or PACING PSI KIT: 5 FR. The batch numbers listed in the recall include specific sequences like 10801902210217, 33F24G0127, etc.
Look for the model numbers on the kit: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, or PACING PSI KIT: 5 FR.
Reach out to Arrow International LLC for more information about the recall and potential remedies.
The supplier had quality issues that could compromise the sterility of the medication, which might lead to serious or life-threatening injuries if the solution is not sterile.
Check the product label for model numbers: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, or PACING PSI KIT: 5 FR. The batch numbers listed in the recall include specific sequences like 10801902210217, 33F24G0127, etc.
Contact Arrow International LLC for more information about the recall and potential remedies.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2366-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2366-2026 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.
