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

Recalled May 13, 2020 · FDA recall Z-1850-2020 · Epimed International

Hazard

Incorrect expiration date on introduction cannula packaging. · FDA Class II

Units

701

Sold at

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.

Description

Incorrect expiration date on introduction cannula packaging.

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.

Manufacturer(s)

Epimed International

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →