Arrow International central venous catheter kits recalled for compromised sterility and drug ineffectiveness
Arrow International catheter kits recalled for sterility risk
Arrow International included injectable anesthetic and saline solutions from a supplier with quality issues in multiple central venous catheter kits and trays. The supplier's products may not be sterile or may not work as intended. If sterility is compromised, these injectable products could cause serious infection or other life-threatening complications.
- Stop using affected Arrow International PSI and MAC catheter kits immediately.
- Contact your hospital or clinic's medical device or procurement department to identify whether you have affected lots.
- Do not use the injectable lidocaine, bupivacaine, or saline from these kits.
- Return affected kits to Arrow International or your supplier for a replacement.
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-2385-2026More Arrow recalls
- FDA-Device2026-06-24Arrow International hemodialysis kits recalled for contaminated anesthetic and saline solutions
- FDA-Device2026-06-24Arrow International PI CVC kits recalled for compromised sterility and drug ineffectiveness
- FDA-Device2026-06-24Arrow International PICC kits and stylets recalled for compromised sterility and drug ineffectiveness
- FDA-Device2026-06-24Arrow International PICC and JACC catheter kits recalled for contaminated anesthetic and saline components
- FDA-Device2026-06-24Arrow International Pacing PSI Kits recalled for potential drug ineffectiveness and sterility compromise
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