CLASS II ONGOING Device recall · Reported 3 Jun 2020 · FDA Enforcement Report
Kangaroo 924 Safety Screw Spike Set, Product recalled by Cardinal Health
Cardinal Health is recalling Kangaroo 924 Safety Screw Spike Set, Product. The recall was initiated on 26 Dec 2019 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2105-2020
- FDA event ID
- 84656
- Recalling firm
- Cardinal Health, Dublin, OH
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 26 Dec 2019
- FDA classified
- 22 May 2020
- Reported
- 3 Jun 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Device type
- Other Medical Devices
Timeline
| 26 Dec 2019 | Recall initiated by company | |
| 22 May 2020 | Classified by FDA | +148 days |
| 3 Jun 2020 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The feeding spike sets may leak at the interface of the tube and spike connector.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Kangaroo 924 Safety Screw Spike Set, Product Code 775759
Where it was distributed
Worldwide distribution.
Questions about this recall
Is Kangaroo 924 Safety Screw Spike Set, Product recalled?
Yes. Cardinal Health recalled Kangaroo 924 Safety Screw Spike Set, Product on 26 Dec 2019. The recall is Class II and its status is Ongoing. Recall number Z-2105-2020.
Why was it recalled?
The feeding spike sets may leak at the interface of the tube and spike connector.
Which lots are affected?
All
Where was it sold?
Worldwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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