FDA Device recall Z-2672-2020
ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM
- FDA Device
- Class II
- terminated
- Published 2020-07-29
On 2020-07-29 the FDA classified a Class II recall of ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM by U And I, citing 6.0x50mm poly-reduction screws were laser etched 6.0x45.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2672-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-05-26 |
| Published | 2020-07-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | U And I |
| Distribution | AZ |
Product
ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM
Reason
6.0x50mm poly-reduction screws were laser etched 6.0x45
Identifiers
| code_info | Lot #: 19C12063 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2672-2020%22
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