Z-2101-2020 Class II Ongoing
FDA device recall Z-2101-2020 was initiated by Cardinal Health Inc. on December 26, 2019 and is designated Class II. Reason for recall: The feeding spike sets may leak at the interface of the tube and spike connector. The recall status is ongoing. Affected quantity: 114,731, 290 total units.
Recall Details
- Product Type
- Devices
- Report Date
- June 3, 2020
- Initiation Date
- December 26, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 114,731, 290 total units
Product Description
Kangaroo Joey Safety Screw Spike Set, Anti-free Flow, Product Code 765559
Reason for Recall
The feeding spike sets may leak at the interface of the tube and spike connector.
Distribution Pattern
Worldwide distribution.
Code Information
All