FDA Device recall Z-2102-2020
Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
- FDA Device
- Class II
- ongoing
- Published 2020-06-03
On 2020-06-03 the FDA classified a Class II recall of Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD by Cardinal Health, citing the feeding spike sets may leak at the interface of the tube and spike connector.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2102-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-12-26 |
| Published | 2020-06-03 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cardinal Health |
| Distribution | n/a |
Product
Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
Reason
The feeding spike sets may leak at the interface of the tube and spike connector.
Identifiers
| code_info | All |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2102-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.