Arrow recalls specific medical kits due to potential contamination in lidocaine, bupivacaine, and saline solutions. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits include 1L, 2L, and 3L sizes with specific model 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 certain medical kits that contain lidocaine, bupivacaine, and saline solutions. The supplier had quality issues that could lead to contaminated products, which might cause serious or life-threatening injuries if the solution's sterility is compromised.
The supplier had quality issues that could compromise the sterility of the water-based injectable solutions. If the solution is not sterile, it could lead to serious infections or life-threatening reactions when injected into the body.
Healthcare professionals and patients who use these kits for medical procedures are at risk. The most vulnerable are those who have received the recalled kits for injections or surgeries.
Check for model numbers like PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC or PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC. The kits were sold with specific batch numbers and lot codes listed in the recall notice.
Discard any recalled medical kits that contain lidocaine, bupivacaine, or saline solutions with the model numbers listed in the recall.
The affected kits include PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC and PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC, among other sizes and model numbers listed in the recall notice.
The supplier had quality issues that could compromise the sterility of the water-based injectable solutions, potentially leading to serious or life-threatening injuries if the solution is not sterile.
Check the model number and batch code on your kit. The recall includes specific model numbers like PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC and batch numbers such as 10801902193275/33F24J0142.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2379-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2379-2026 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.
