Kangaroo Connect ENPlus Spike Set Anti-free Flow — Class II medical device recall Z-2102-2020
Ongoing recall by Cardinal Health Inc., reported 2020-06-03. The feeding spike sets may leak at the interface of the tube and spike connector.
| Recall number | Z-2102-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health Inc., Dublin, OH, United States |
| Recall initiated | 2019-12-26 |
| Classified | 2020-05-22 |
| Reported by FDA | 2020-06-03 |
| Reason classes | packaging |
Product
Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
Reason for recall
The feeding spike sets may leak at the interface of the tube and spike connector.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2102-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.