Z-2105-2020 Class II Ongoing
FDA device recall Z-2105-2020 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 924 Safety Screw Spike Set, Product Code 775759
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