CLASS II Food recall · Reported 19 Feb 2020 · FDA Enforcement Report

bliss anti-stress formula Dietary Supplement recalled by Market America

Market America is recalling bliss anti-stress formula Dietary Supplement, distributed in 46 states. The recall was initiated on 19 Oct 2017 and the FDA has classified it as Class II.

Check your package

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

Quantity recalled1,496/60 tablet bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0681-2020
FDA event ID: 84537
Recalling firm: Market America, Greensboro, NC
Classification: Class II
Status: Completed
Recall initiated: 19 Oct 2017
FDA classified: 10 Feb 2020
Reported: 19 Feb 2020
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Allergens
Product category: Dietary Supplements

Timeline

19 Oct 2017	Recall initiated by company
10 Feb 2020	Classified by FDA	+844 days
19 Feb 2020	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

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.

Alaska Alabama Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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