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Kimberly-Clark Corporation recalls Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Ki
Recalled February 5, 2014 · FDA recall Z-0850-2014 · Kimberly-Clark
Hazard
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label. · FDA Class II
Units
55 cases (10 units per case = 550 units)
Sold at
US Distribution in states of: AZ, CA, DE, FL, LA, MD, MA, NJ, NY, OH, PA and TX.
Description
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
Product
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.
Manufacturer(s)
Kimberly-Clark Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →