Arrow International midline and central venous catheter kits recalled for contaminated anesthetic and saline components
What this means
Arrow International catheter kits contain lidocaine, bupivacaine, and saline solution from a supplier with quality control issues. The supplier's products may not be sterile or effective. If these injectable components are contaminated, they could cause serious or life-threatening infections.
- Stop using affected catheter kits immediately if you have one in your facility.
- Check the product lot numbers on your kits against the recalled batches.
- Contact Arrow International or your supplier for instructions on returning or replacing affected kits.
- Report any patient injuries or product issues to the FDA MedWatch program.
The agency's original wording
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2394-2026Want us to check the next one for you?
We read every CPSC, FDA, USDA, and NHTSA notice and email you a plain-English Sunday brief covering your household — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.