The Recall Desk
HighFDA (Devices)·Z-2717-2017·Announced 2017-07-19

ICU Medical Recalls Smallbore Extension Sets Due to Potential Leak

ICU Medical is recalling 120 units of smallbore extension sets because the connection between the Female Luer and NanoClave manifold may develop a 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: The recall is classified as FDA Class II, and the hazard involves a potential leak in a medical device used for vascular fluid administration, which poses a risk of harm to patients even though no specific injuries are reported in the source text.

Plain-English summary

ICU Medical, Inc. is recalling 120 units of 168 cm (66") PVC/PUR Smallbore Extension Sets with 6-Port NanoClave Manifold, Check Valve, MicroClave Clear, and Rotating Luer. The affected products are identified by Item No. 011-AM6115 and Lot Nos. 3297341, 3354442, and 3388890. These devices are single-use, sterile, non-pyrogenic medical devices used to provide access for the administration of fluids from a container to a patient's vascular system.

The recall was initiated because the connection between the Female Luer and the NanoClave manifold has the potential for developing a leak. This defect could compromise the integrity of the fluid administration system.

The affected units were distributed to Italy and France, as well as the following US states: Arizona, Ohio, Texas, and Washington. Healthcare facilities and consumers who have these specific lot numbers should stop using the devices and contact ICU Medical for further instructions.

The recalled product

Product
168 cm (66") Appx 2.6 ml, PVC/PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, MicroClave¿ Clear, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container t
Manufacturer
ICU Medical, Inc.
Category
Medical Device — IV Administration Sets
Hazard
Affected units
120

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 No. 3297341
  • 3354442
  • 3388890. Item No. 011-AM6115

Distribution

Distributed in 4 states:

Part of a larger recall action

This product is one of 9 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 9 products in this recall →

Related recalls

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Same hazard · leak

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