FDA Device recall Z-0452-2021
Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery o…
- FDA Device
- Class II
- ongoing
- Published 2020-11-25
On 2020-11-25 the FDA classified a Class II recall of Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery o… by Cardinal Health 200, 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-0452-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-09-22 |
| Published | 2020-11-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.
Reason
The feeding spike sets may leak at the interface of the tube and spike connector.
Identifiers
| code_info | All lots of products manufactured in the below timespan: July 1, 2015 and July 20, 2019 |
|---|
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-0452-2021%22
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