Cardinal Health Recalls Kangaroo Connect 500ml Bag Sets Due to Leakage
Cardinal Health is recalling Kangaroo Connect 500ml Bag Sets because they may leak at the tube and spike connector interface.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device used for nutritional feeding that may leak, posing a risk of harm, but the source text does not report any specific injuries or illnesses.
Plain-English summary
Cardinal Health 200, LLC is recalling Kangaroo Connect 500ml Bag Sets, Non-Sterile, Product Code 77500FD. These single-use tubing sets are used with pumps for the delivery of nutritional feeding products.
The recall is being issued because the feeding spike sets may leak at the interface of the tube and spike connector. The affected units were manufactured between July 1, 2015, and July 20, 2019, and were distributed nationwide in the United States.
Consumers should stop using the affected products and contact Cardinal Health for further instructions or a refund.
The recalled product
- 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.
- Manufacturer
- Cardinal Health 200, LLC
- Category
- Medical Device — Feeding Tubes
- Hazard
- Affected units
- 314,460
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All lots of products manufactured in the below timespan: July 1
- 2015 and July 20
- 2019
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Cardinal Health 200, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Cardinal Health 200, LLC
See all →- HighCardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
FDA (Devices) · 2026-08-19
- HighCardinal Health Recalls Neurological Procedure Kits Due to Endotoxin Variability
FDA (Devices) · 2026-08-19
- HighCardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
FDA (Devices) · 2026-08-19
- HighCardinal Health Presource Kits Recalled for Endotoxin Variability
FDA (Devices) · 2026-08-19
- HighCardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
FDA (Devices) · 2026-08-19
Same hazard · leakage
See all →- HighConvaTec Esteem Body Soft Convex Urostomy Pouches Recalled for Leakage
FDA (Devices) · 2026-08-26
- SevereStryker AHTO Tube Set Packaging Recalled for Handpiece Leaking
FDA (Devices) · 2026-08-12
- SevereMedtronic Perfusion Systems Recalls EOPA Elongated One-Piece Arterial Cannula Model 77522
FDA (Devices) · 2026-08-05
- HighICU Medical Recalls Hotline Fluid Warming Sets Due to Leakage Risk
FDA (Devices) · 2026-07-29
- SevereABIOMED Introducer Kit 23 Fr heart pump accessory leakage risk
FDA (Devices) · 2026-07-22