Cardinal Health Inc. Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
Brand
Cardinal Health Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All
Cardinal Health Inc. is recalling Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD due to The feeding spike sets may leak at the interface of the tube and spike connector.. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: specific lot/serial numbers.
Reason for Recall
As stated by FDA
The feeding spike sets may leak at the interface of the tube and spike connector.
Recommended Action
Per FDA guidance
A Medical Device Product Advisory letter dated 12/23/19 was sent to customers. 1) INSPECT your inventory for affected product. 2) COMMUNICATE with all personnel that utilize the equipment the risk of leaks at the interface of the tube and spike connector. 3) INSPECT the feeding set for leaks after the pump has been primed and the infusion has started. " If a leak is detected the feeding set must be discarded and a new feeding set must be obtained. Inspect the new feeding set for leaks in the same manner. 4) NOTIFY any customers to whom you may have distributed or forwarded affected product about this product advisory. 5) RETURN the enclosed acknowledgment form via fax to 847-689-9101 or 614-652-9648 or email to gmb-fieldcorrectiveaction@cardinalhealth.com, whether or not you have affected product. Please contact the Customer Service group for any questions related to this action: " Hospital800-964-5227 " Federal Government800-444-1166 " Distributor800-635-6021 " All other customers888-444-5440 For questions related to the notification and/or acknowledgement form that are not adequately addressed in this letter, please contact the market action team at: GMB-FieldCorrectiveAction@cardinalhealth.com or call 800-292-9332.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026