Class IICompleted in FDA datasetRecall initiated Oct 19, 2017

bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and

Recalling firm: Market America Inc

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Completed” describes the FDA recall process; it does not certify that an individual package is safe.

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Productbliss 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
UPC848570004703

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC848570004703d by: Market America, Inc., 1302 Pleasant Ridge Road, Greensboro, NC 27409; UPC 8 48570 00470 3

Original FDA recall reason

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

Recall details

Recall number
F-0681-2020
Event ID
84537
FDA status
Completed
Initiated
Oct 19, 2017
Reported
Feb 19, 2020
Classified
Feb 10, 2020
Quantity
1,496/60 tablet bottles
Location
Greensboro, NC, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was 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.

FDA source record · F-0681-2020

Data updated September 16, 2026. View official FDA data ↗

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