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ARROW INTERNATIONAL, LLC recalls Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
Recalled June 24, 2026 · FDA recall Z-2380-2026 · ARROW INTERNATIONAL
Hazard
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. · FDA Class I
Units
7560
Sold at
US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.
Description
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.
Product
Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
Manufacturer(s)
ARROW INTERNATIONAL, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →