RecallRadar

FDA Food recall F-0681-2020

bliss anti-stress formula Dietary Supplement, 60 Tablets

On 2020-02-19 the FDA classified a Class II recall of bliss anti-stress formula Dietary Supplement, 60 Tablets by Market America, citing potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.

Read the official FDA Food notice

AgencyFDA Food
Recall numberF-0681-2020
ClassificationClass II
Statuscompleted
Initiated2017-10-19
Published2020-02-19
Last updated2026-09-13 11:50 UTC
CompanyMarket America
DistributionAK, 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, VT, WA, WI, WV

Product

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

Reason

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

Identifiers

upc848570004703
code_infoLot #: 51130, Expiration Date: 07/2019 Manufacturer's Code PK-MA13173 Manufacturer's Item #Z02320

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: completed.

Source

Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0681-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.