Arrow recalls PARACENTESIS KIT (ASK-0:00376-JHH) due to potential contamination in lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if sterility is compromised.
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 PARACENTESIS KITS with specific serial numbers because the drugs inside may be contaminated, which could lead to serious or life-threatening injuries if the sterility is compromised.
The kits contain lidocaine, bupivacaine, and saline solutions that may have been contaminated by the supplier. If the sterility of these injectable drugs is compromised, it could lead to serious or life-threatening infections or reactions.
Medical professionals who use these kits for procedures like paracentesis are most at risk. Patients receiving the kits could also be affected if the drugs are contaminated.
Check for the serial numbers 10801902193275 and 33F25G0629, 33F24K0592 on the kit packaging. These kits were sold with the reference code ASK-00376-JHH.
Immediately stop using the recalled PARACENTESIS KIT with the serial numbers 10801902193275 and 33F25G0629, 33F24K0592.
The supplier had quality issues with the drugs in the kit, which could lead to serious or life-threatening injuries if the sterility is compromised.
The kit contains lidocaine, bupivacaine, and 0.9% sodium chloride solutions.
Check for the serial numbers 10801902193275 and 33F25G0629, 33F24K0592 on the kit packaging.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2386-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2386-2026 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.
