Bliss anti-stress formula Dietary Supplement recalled over undeclared yohimbe
- Recall date
- October 19, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Market America Inc recalls bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc., 13…
- Recall number
- F-0681-2020
- FDA classification
- Class II
- Brand / firm
- Market America Inc
- Sold / distributed
- Product was shipped to the following states: AK, AL, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI & WV. Product was also shipped to Australia, Canada & Hong Kong.
Why it was recalled
Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc., 1302 Pleasant Ridge Road, Greensboro, NC 27409; UPC 8 48570 00470 3
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