Food Recall Check
Class II · Moderate risk Completed Initiated Oct 19, 2017 (9 years ago)

bliss anti-stress formula Dietary Supplement recall

Recalled by Market America Inc · Greensboro, NC, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.

See the recall's own reason text for the specifics. All other reasons recalls.

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

Quantity: 1,496/60 tablet bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot #: 51130, Expiration Date: 07/2019 Manufacturer's Code PK-MA13173 Manufacturer's Item #Z02320

Where it was sold

Alaska Alabama Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia

FDA's distribution note: 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.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as completed: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Market America Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 19, 2017
In FDA report of
Feb 19, 2020
FDA recall number
F-0681-2020 · event 84537
Official record
FDA enforcement report search

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