Durisan Hand Sanitizer Recall Due to Microbial Contamination with Burkholderia cepacia complex and Ralstonia pickettii

The FDA announced that Sanit Technologies LLC doing business as Durisan, recalled many Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes. The recall is due to out-of-specification results for bacterial count for Burkholderia cepacia complex and Ralstonia pickettii. The issue was discovered during a routine audit focused on production scale-up during the height of the pandemic. No adverse reactions were reported. The product was packaged in sizes ranging from 18mL credit cards to bottles sized in 118, 236, 300, and 550 mL and 1000mL wall-mounted dispenser refills. The product was manufactured from Feb. 1, 2020, until June 30, 2020, and distributed to selected retailers nationwide in the United States. @ https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/durisan-hand-sanitizer-recall-due-microbial-contamination?utm_medium=email&utm_source=govdelivery