ICU Medical ChemoLock Port REF: CL2100

FDA Recall #Z-0350-2026 — Class II — September 8, 2025

Recall #Z-0350-2026 Date: September 8, 2025 Classification: Class II Status: Ongoing

Product Description

ICU Medical ChemoLock Port REF: CL2100

Reason for Recall

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

Recalling Firm

ICU Medical, Inc. — San Clemente, CA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

133,255 units

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.

Code Information

UDI:10887709057002/Lot:14400191, 14379145

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

Back to All Device Recalls