Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Kimberly-Clark RadiOpaque Radiofrequency Cannula Recalled by Kimberly-Clark Corporation Due to Product may contain a cannula with an active...
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 Kimberly-Clark Corporation directly.
Affected Products
Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code PMF22-100-10 The product is used to create lesions in nervous tissue when used with the Kimberly-Clark radiofrequency generator and probes.
Quantity: 55 cases (10 units per case = 550 units)
Why Was This Recalled?
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
Where Was This Sold?
This product was distributed to 12 states: AZ, CA, DE, FL, LA, MD, MA, NJ, NY, OH, PA, TX
About Kimberly-Clark Corporation
Kimberly-Clark Corporation has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report