Reported May 13, 2020 · Terminated
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 -…
Epimed International
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Epimed International · 13958 Diplomat Dr · Farmers Branch, TX · 75234-8805
Is this the product you have?
- R-F Injector Cannula. 18gx10cm-STERILE
- REF/UDI257-1810/(01)00828788021496
- REF/UDI257-1810D(01)10818788021493 -
- Product UsageThe Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Product as published — 14108679/exp. 3-29-23/ — 14109199/exp. 1-21-24/ 257-1810D14108568/exp. 2-4-23/ Sterile Lot #/Expiration Date/ — 14109199/ exp. 1-21-24/ — 14109690/exp. 9-26-24/ - Amount recalled
- 1374
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Incorrect expiration date on introduction cannula packaging.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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