Cardinal Health Recalls Kangaroo Epump Safety Screw Spike Sets
Cardinal Health 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 the hazard involves a potential leak in a medical device, which poses a risk of harm even though specific injuries are not reported in the source text.
Plain-English summary
Cardinal Health Inc. is recalling Kangaroo Epump Safety Screw Spike with Flush Bag, Anti-free Flow, 1000 mL, Product Code 775100. The recall involves 114,731 units of this specific product code, with a total of 290 units affected across all codes. The products were 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 medical device during use.
Healthcare providers and consumers should stop using the affected products immediately. Cardinal Health is the recalling firm responsible for managing the recall process.
The recalled product
- Product
- Kangaroo Epump Safety Screw Spike with Flush Bag, Anti-free Flow, 1000 mL, Product Code 775100
- 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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