Z-1725-2021 Class II Terminated
FDA device recall Z-1725-2021 was initiated by Zavation on March 25, 2021 and is designated Class II. Reason for recall: Products distributed as sterile may not have been adequately sterilized The recall status is terminated (terminated March 20, 2023). Affected quantity: 27 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 9, 2021
- Initiation Date
- March 25, 2021
- Termination Date
- March 20, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 27 units
Product Description
ZVplasty Directional Cement Cannula Long, REF VCF-1080-L. For use in Orthopedic / spinal procedures.
Reason for Recall
Products distributed as sterile may not have been adequately sterilized
Distribution Pattern
US nationwide distribution.
Code Information
Lot: 20061365