FDA recall Z-0365-2026

ICU Medical, Inc. · Class II · device

Product

ICU Medical ChemosafeLock Vial Adapter REFs: KL-VA001U3 KL-VA002U3 KL-VA131U3 KL-VA201U3 KL-VA202U3 KL-VA321U3

Reason for recall

Port weld of drug transfer device may separate or break during use and potentially result in a leak.

Distribution

Worldwide distribution: US (Nationwide) including states of: AK AL AR AZ CA CO CT DE FL GA IA ID IL KS KY LA MA MD MI MN MS MT NC NE NJ NM NV NY OH OK OR PA SD TN TX VA WA WY and OUS (foreign) to countries of: Canada, France, and Japan.

Key facts

Status: Ongoing
Initiation date: 2025-09-08
Report date: 2025-11-05
Voluntary/Mandated: Voluntary: Firm initiated
Location: San Clemente, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0365-2026