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Lower risk Medical device recall · FDA · Published December 26, 2019

Cardinal Health Kangaroo Connect Spike Set May Leak at Tube Connection

Cardinal Health recalls Kangaroo Connect ENPlus Spike Set Anti-free Flow (Product Code 77000FD) due to potential leaks at the tube and spike connector interface. All units are affected.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2102-2020Medical deviceCardinal Health ›
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Contact the company

Recalling firmCardinal Health Inc.7000 Cardinal Pl · Dublin, OH 43017-1091
✎ GovInfoNow plain-language explainer

Cardinal Health is recalling all Kangaroo Connect ENPlus Spike Set Anti-free Flow products (Product Code 770:00FD) because they may leak at the connection between the tube and spike. This leak could cause the product to malfunction or cause injury if the fluid leaks onto the user. Read more at govinfonow.com/recall/66201-cardinal-health-kangaroo-connect-spike-set-may-leak-at-tube.

Source Summary by GovInfoNow · govinfonow.com/recall/66201-cardinal-health-kangaroo-connect-spike-set-may-leak-at-tube · Updated September 23, 2026 · FDA enforcement record: FDA #Z-2102-2020

Cite this page

“Cardinal Health Kangaroo Connect Spike Set May Leak at Tube Connection.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/66201-cardinal-health-kangaroo-connect-spike-set-may-leak-at-tube. Based on FDA recall #Z-2102-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2102-2020%22&limit=1).

The FDA announced on 2019-12-26 that Cardinal Health Inc. is recalling Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD, because the feeding spike sets may leak at the interface of the tube and spike connector.

How to tell if you have it

  • Brand: Cardinal Health
  • Product: Kangaroo Connect ENPlus Spike Set Anti-free Flow
  • Product Code: 77000FD

The hazard

The feeding spike sets may leak at the interface of the tube and spike connector, according to the FDA.

Context

GovInfoNow's records show Cardinal Health Inc. has 11 other recalls on record since 2018-11-16. Other recent recalls include Enoxaparin 30mg Syringes recalled on 2025-08-05 due to wrong labeling, RECOMBINATE Antihemophilic Factor recalled on 2025-07-30 for temperature exposure risk, and Wegovy injection recalled on 2025-04-09 for temperature abuse risk. Other recent recalls of similar products include Medline ENFIT G-Tube Connectors (2026-02-13), Stryker Single Spike Tube Set (2026-06-08), and Stryker Ahto Dual Spike Tube Set (2026-06-08).

How to tell if you have this one

Check for the product name 'Kangaroo Connect ENPlus Spike Set Anti-free Flow' and product code 77000FD. All units are affected, so no specific model or purchase date is needed.

  • Brand
    Cardinal Health
  • Category
    Medical device
FDA recall event · 6 products

All 6 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
    Worldwide distribution.
Recall numberProduct, codes & lots
Z-2100-2020Kangaroo Joey Safety Screw Spike with Flush Bag, Anti-free Flow,1000 mL, Product Code 765100; All
Z-2101-2020Kangaroo Joey Safety Screw Spike Set, Anti-free Flow, Product Code 765559; All
Z-2102-2020Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD; All
Z-2103-2020Kangaroo Epump Safety Screw Spike with Flush Bag, Anti-free Flow, 1000 mL, Product Code 775100; All
Z-2104-2020Kangaroo Epump Safety Screw Spike Set, Anti-free Flow, Product Code 775659; All
Z-2105-2020Kangaroo 924 Safety Screw Spike Set, Product Code 775759; All
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name 'Kangaroo Connect ENPlus Spike Set Anti-free Flow' and product code 77000FD.

How this recall unfolded

Recall timeline

FDA published this recall 5 months after the firm started it.

1. Firm started the recall: Dec 26, 201912. FDA classified it Class II: May 22, 202023. Published in FDA’s Enforcement Report: Jun 3, 2020320192020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Cardinal Health Inc. recalls LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle,
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Where this comes from

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-2102-2020 (December 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2102-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on September 23, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA