Use cautionMedical device recall · FDA · Published September 22, 2020
Kangaroo Connect 1000ml Bag Set Leak Risk - Recall for Feeding Spikes
Cardinal Health recalls Kangaroo Connect 1000ml Bag Sets due to potential leaks at tube-spike connectors. Affected units made between July 2015 and July 2019. Stop using immediately to prevent feeding errors.
The feeding spike sets may leak at the interface of the tube and spike connector.
Take action
Contact the company
📍Recalling firmCardinal Health 200, LLC15 Hampshire St Bldg 5 · Mansfield, MA 02048-1113
✎ GovInfoNow plain-language explainer
Cardinal Health is recalling Kangaroo Connect 1000ml Bag Sets that may leak at the tube and spike connector. This leak risk could cause feeding errors if the bag is used with pumps for nutritional delivery. Affected units were made between July 2015 and July 2019. Read more at govinfonow.com/recall/64231-kangaroo-connect-1000ml-bag-set-leak-risk-recall-for-feeding.
“Kangaroo Connect 1000ml Bag Set Leak Risk - Recall for Feeding Spikes.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64231-kangaroo-connect-1000ml-bag-set-leak-risk-recall-for-feeding. Based on FDA recall #Z-0453-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0453-2021%22&limit=1).
Cardinal Health 200, LLC voluntarily recalled Kangaroo Connect 1000ml Bag Sets due to potential leakage at the tube and spike connector interface, the FDA said on Sept. 22, 2020.
How to tell if you have it
Brand: Cardinal Health
Product: Kangaroo Connect 1000ml Bag Set, Non-Sterile
Product Code: 77100FD
Lot dates: July 1, 2015 through July 20, 2019
Distribution: US Nationwide
The hazard
The feeding spike sets may leak at the interface of the tube and spike connector.
Context
GovInfoNow's records show Cardinal Health 200, LLC has issued 59 other recalls since June 27, 2017. Other recent recalls include Presource Packs with Microstream Components (Aug. 19, 2026), Presource Gyn Laparoscopy Kits (Aug. 18, 2026), and Presource Convenience Kits (Aug. 10, 2026). Similar product recalls include Stryker Single Spike Tube Set (June 8, 2026), Stryker Ahto Dual Spike Tube Set (June 8, 2026), and ICU Medical Hotline Fluid Warming Set (June 24, 2026).
How to tell if you have this one
Check for the product code 77100FD on the Kangaroo Connect 1000ml Bag Set. Units were manufactured between July 1, 2015 and July 20, 2019.
Brand
Cardinal Health
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution.
Recall number
Product, codes & lots
Quantity
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.; All lots of products manufactured in the below timespan: July 1, 2015 and July 20, 2019
314460
Z-0453-2021
Kangaroo Connect 1000ml Bag Set, Non-Sterile, Product Code 77100FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.; All lots of products manufactured in the below timespan: July 1, 2015 and July 20, 2019
197370
Based on the official FDA remedy
What to do — step by step
Stop Using Immediately
Discontinue use of the Kangaroo Connect 1000ml Bag Set if it has the product code 77100FD and was manufactured between July 2015 and July 2019.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0453-2021 (September 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0453-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.