Z-2672-2020 Class II Terminated
FDA device recall Z-2672-2020 was initiated by U&I CORP. on May 26, 2020 and is designated Class II. Reason for recall: 6.0x50mm poly-reduction screws were laser etched 6.0x45 The recall status is terminated (terminated April 5, 2024). Affected quantity: 6.
Recall Details
- Product Type
- Devices
- Report Date
- July 29, 2020
- Initiation Date
- May 26, 2020
- Termination Date
- April 5, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6
Product Description
ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM
Reason for Recall
6.0x50mm poly-reduction screws were laser etched 6.0x45
Distribution Pattern
U.S.: AZ
Code Information
Lot #: 19C12063