May 07, 2013

Chang Kwung Recalls Lightning Rod Capsules Due to Undeclared Ingredient

The Missouri Department of Health and Senior Services received information regarding a recall of dietary supplements sold under the brand name Lightning Rod 500 mg per capsule packaged in 3-count, UPC 6 89076 20257 2 and 12-count bottles, UPC 6 89076 20297 8.Testing found the Lightning Rod Capsules to contain an analogue of Sildenafil, an active ingredient for the treatment of male Erectile Dysfunction.

Lightning Rod capsules are sold over the counter as a dietary supplement marketed for male sexual enhancement. It is sold nationwide via internet in 3 capsule count and 12 capsule count bottles between August 2012 and May 3, 2013.

The full recall can be found at www.fda.gov/Safety/Recalls/ucm351058.htm.


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