The Recall Desk
ModerateFDA (Devices)·Z-1999-2020·Announced 2020-05-20

ICU Medical Recalls Central Venous Catheters Due to Guidewire Issue

ICU Medical is recalling 60 units of Model 41406-23 Central Venous Catheters because the included guidewires cannot pass through the needles.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the defect is a functional failure (guidewire cannot pass through needle) rather than a direct safety hazard like infection or injury, fitting the Moderate criteria for low-risk functional issues.

Plain-English summary

ICU Medical, Inc. is recalling 60 units of Central Venous Catheters, Model # 41406-23. These devices are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring.

The recall is due to an inability for the guidewire to pass through the needles included with the catheter kits. The affected units were distributed to US consignees in Alabama, California, Florida, Georgia, Illinois, Maine, Michigan, Minnesota, Mississippi, North Carolina, New Hampshire, New Mexico, New York, Ohio, Texas, Utah, Virginia, and Washington, as well as to consignees in Canada.

Healthcare facilities and consumers should stop using the affected devices and contact ICU Medical for further instructions.

The recalled product

Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41406-23
Manufacturer
ICU Medical, Inc.
Category
Medical Device — Catheters
Hazard
Affected units
60

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 (2)

  • LOT Number/ UDI-4155999/1 0840619 04642 9
  • 4192320/1 0840619 04642 9

Distribution

Distributed in 19 states:

Part of a larger recall action

This product is one of 7 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 7 products in this recall →

Related recalls

Same manufacturer · ICU Medical, Inc.

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Same hazard · functional defect

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