Cardinal Health Recalls Kangaroo Connect ENPlus Spike Sets for Leaking
Cardinal Health is recalling Kangaroo Connect ENPlus Spike Sets because they may leak at the tube and spike connector interface.
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 involves a medical device defect (leaking) that poses a risk of harm, but no specific injuries or illnesses are reported in the source text.
Plain-English summary
Cardinal Health Inc. is recalling Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD. The recall involves 114,731 units, with a total of 290 units distributed worldwide.
The recall was initiated because the feeding spike sets may leak at the interface of the tube and spike connector. This defect could potentially compromise the integrity of the feeding system.
Consumers and healthcare providers who have these products should stop using them and contact Cardinal Health for further instructions or a replacement.
The recalled product
- Product
- Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
- Manufacturer
- Cardinal Health Inc.
- 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)
- All
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 6 recalled by Cardinal Health 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.
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