The Recall Desk
HighFDA (Devices)·Z-0361-2026·Announced 2025-11-05

Six inch extension sets recalled because port weld may separate and leak

ICU Medical is recalling 1,600 6-inch extension sets with MicroClave Clear and ChemoLock port because the port weld of the drug transfer device may separate or break during use and leak.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Scored 3 under the risk-of-harm criterion: a weld that can break and leak on a drug transfer device is a hazard, and no injuries are reported.

Plain-English summary

The ICU Medical 6 inch (15 cm) extension set with MicroClave Clear, ChemoLock Port, Y-Connector and rotating Luer, REF CL4118, is being recalled.

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

The recall covers 1,600 units from lots 14393173 and 14409213. Distribution was worldwide, including nationwide in the United States and Canada. The FDA has classified the action as Class II.

The enforcement record describes the weld failure and reports no injuries. Because these sets are used to transfer hazardous drugs, facilities should quarantine affected lots and follow ICU Medical's instructions.

The recalled product

Product
ICU Medical 6" (15 cm) Ext Set w/MicroClave" Clear, ChemoLock" Port, Y-Connector, Rotating Luer REF: CL4118
Manufacturer
ICU Medical, Inc.
Affected units
1,600

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lot:14393173
  • 14409213
  • Distributed in Canada

Distribution

Distributed nationwide across the United States.

The notice also names 38 states specifically:

Part of a larger recall action

This product is one of 38 recalled by ICU Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 38 products in this recall →