Epimed International: Medical Device Recall in 2020 - (Recall #: Z-1849-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: February 21, 2020

Date Posted: May 13, 2020

Recall Number: Z-1849-2020

Event ID: 85339

Reason for Recall:

Incorrect expiration date on introduction cannula packaging.

Status: Terminated

Product Quantity: 1374

Code Information:

Catalog #257-1810 Sterile Lot #/Expiration Date/ 1. 14108679/exp. 3-29-23/ 2. 14109199/exp. 1-21-24/ 3. 14108568/exp. 2-4-23/ Catalog #257-1810D Sterile Lot #/Expiration Date/ 1. 14109199/ exp. 1-21-24/ 2. 14109690/exp. 9-26-24/

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated