# FDA recall Z-1850-2020

> **Epimed International** · Class II · device recall initiated 2020-02-21.

## Product

R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124; REF/UDI: 257-2010D(01)00818788022127 - 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.

## Distribution

Worldwide distribution - US Nationwide distribution including the states of AL, CA, FL, GA, IL, MD,MI, MS, NJ, NY, OK,  TN, TX, WA and WY and the countries of Australia, Chile, United Kingdom.

## Key facts

- **Recall number:** Z-1850-2020
- **Recalling firm:** Epimed International
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-21
- **Report date:** 2020-05-13
- **Termination date:** 2021-01-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Farmers Branch, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1850-2020

## Citation

> AI Analytics. FDA recall Z-1850-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-1850-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*