ANAX 5 — Class II medical device recall Z-2672-2020
Terminated recall by U&I CORP., reported 2020-07-29, distributed in AZ. 6.0x50mm poly-reduction screws were laser etched 6.0x45
| Recall number | Z-2672-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | U&I CORP., Uijeongbu, N/A, Korea (the Republic of) |
| Recall initiated | 2020-05-26 |
| Classified | 2020-07-20 |
| Reported by FDA | 2020-07-29 |
| Terminated | 2024-04-05 |
| Distributed | AZ |
| Quantity | 6 |
| Lot numbers | 19C12063 |
| Model numbers | SFNA6050R |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2672-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.