Z-2052-2019 Class II
FDA device recall Z-2052-2019 was initiated by Cardinal Health 200, LLC on April 30, 2019 and is designated Class II. Reason for recall: Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- July 31, 2019
- Initiation Date
- April 30, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
Reason for Recall
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Distribution Pattern
Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL
Code Information
Lot Number: 903530