Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496 Recalled by Epimed International Due to Incorrect expiration date on introduction cannula packaging.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Epimed International directly.
Affected Products
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.
Quantity: 1374
Why Was This Recalled?
Incorrect expiration date on introduction cannula packaging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Epimed International
Epimed International has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report