FDAFebruary 21, 2020device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Incorrect expiration date on introduction cannula packaging.

What to do

FDA enforcement status: Terminated

Brands named

epimed

UPCs

0082878802149610818788021493

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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