The Recall Desk
HighFDA (Devices)·Z-0272-2021·Announced 2020-10-28

ICU Medical Recalls APPX NanoClave Manifold Sets Due to Seal Defect

ICU Medical is recalling specific lots of APPX 0.75ml NanoClave Manifold sets because a manufacturing defect may prevent a proper seal.

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 involves a medical device with a functional defect that could compromise the integrity of the fluid administration system, representing a risk of harm where injury has not yet been reported.

Plain-English summary

ICU Medical, Inc. is recalling specific lots of APPX 0.75ml, 6-Port NanoClave Manifold sets. The recall involves a total of 304,735 units distributed worldwide, including the United States and several international countries. The affected product is identified by Lot Number 4496182.

The recall was initiated due to a potential manufacturing defect on the internal surface of the NanoClave component. This defect may inhibit a proper seal with the NanoClave spike. Administration sets and their accessories are single-use, pre-sterilized devices used to provide access for the administration of fluids to a patient's vascular system.

Healthcare facilities and distributors should stop using the affected lots and contact ICU Medical for instructions on return or replacement. Consumers should not use these devices if they have them in their possession.

The recalled product

Product
APPX 0.75ml, 6-Port NanoClave Manifold (Glow, Red, Blue, Purple, Yellow Rings)BCV. 1 unit per pouch, 50 pouches per case. UDI: (01)10840619083929(17)241201(30)50(10)4496182. Administration sets and their accessories are single use, pre-sterilized devices that provide access f
Manufacturer
ICU Medical, Inc.
Category
Medical Device — IV Administration Sets
Hazard

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 (1)

  • Lot Number:4496182.

Distribution

Distributed nationwide across the United States.

The notice also names 37 states specifically:

Part of a larger recall action

This product is one of 99 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 99 products in this recall →

Related recalls

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Same hazard · seal defect

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