R-F Injector Cannula — Class II medical device recall Z-1849-2020
Terminated recall by Epimed International, reported 2020-05-13, distributed nationwide. Incorrect expiration date on introduction cannula packaging.
| Recall number | Z-1849-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Epimed International, Farmers Branch, TX, United States |
| Recall initiated | 2020-02-21 |
| Classified | 2020-05-04 |
| Reported by FDA | 2020-05-13 |
| Terminated | 2021-01-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CL, GB |
| Quantity | 1,374 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 10818788021493 |
| Lot numbers | 14108568, 14108679, 14109199, 14109690 |
| Model numbers | 257-1810, 257-1810D |
| Expiration dates | 2023-02-04, 2023-03-29, 2024-01-21, 2024-09-26 |
Product
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
Reason for recall
Incorrect expiration date on introduction cannula packaging.
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-1849-2020. 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.