Cardinal Health Recalls Kangaroo Epump Safety Screw Spike Sets
Cardinal Health Inc. is recalling Kangaroo Epump Safety Screw 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 risk-of-harm product (medical device leak) where specific injury reports are not yet detailed in the source text, fitting the 'High' severity criteria for risk-of-harm products without reported injury.
Plain-English summary
Cardinal Health Inc. is recalling the Kangaroo Epump Safety Screw Spike Set, Anti-free Flow, Product Code 775659. The recall involves 114,731 units, with a total of 290 units distributed worldwide.
The product is being recalled because the feeding spike sets may leak at the interface of the tube and spike connector. This defect could potentially affect the integrity of the medical device during use.
Consumers and healthcare facilities should stop using the affected products and contact Cardinal Health Inc. for further instructions or a replacement.
The recalled product
- Product
- Kangaroo Epump Safety Screw Spike Set, Anti-free Flow, Product Code 775659
- 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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