Arrow International LLC recalls specific catheter kits due to supplier quality issues with lidocaine, bupivacaine, and saline solutions potentially causing 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 International LLC has recalled multiple catheter kits and arterial line kits that contain lidocaine, bupivacaine, and saline solutions. These products were found to have quality issues from a supplier, which could lead to serious or life-threatening injuries if the sterility of the injectable products is compromised.
The supplier of the products had quality issues that could compromise the sterility of the water-based injectable products. If the products are not sterile, they could cause serious or life-threatening injuries when used in medical procedures.
Healthcare professionals who use these catheter kits for medical procedures are most at risk. Patients receiving these kits during procedures may also be affected if the products are used without proper sterility.
Check for the following model numbers: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1; RA CATH KIT: 20 GA X 1 1/2IN/NA-04220-S1A; ARTERIAL LINE KIT/AK-04510-S; and other specific kit models listed in the recall notice.
Look for model numbers like RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 or ARTERIAL LINE KIT/AK-04510-S on the product packaging.
Contact Arrow International LLC for more information about the specific model and how to proceed with the recall.
Arrow recalls specific catheter kits and arterial line kits with model numbers like RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 and ARTERIAL LINE KIT/AK-04510-S.
The supplier had quality issues that could compromise the sterility of the water-based injectable products, which could lead to serious or life-threatening injuries if not properly sterile.
Check the product model number and contact Arrow International LLC for instructions on how to proceed with the recall.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2368-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2368-2026 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.
