Product Wiki · Recalls · U.S. FDA — Device Enforcement

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 of nutritional feeding product.

U.S. FDA — Device Enforcement · United States · 2020-09-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0452-2021
Date of alert
2020-09-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Reported risk: The feeding spike sets may leak at the interface of the tube and spike connector.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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