MyNicNaxs, Inc.

Complete recall history across all FDA and CPSC categories — 10 total recalls

MyNicNaxs, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (10)

FDA drug safety enforcement actions by MyNicNaxs, Inc.

Date Product Reason Class
Jan 24, 2014 Slim Xtreme Weight loss capsules, 500 mg, supplied in 30 count bottles, Anoth... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 Magic Slim capsules, supplied in 60 count bottles, distributed by MyNicKnaxs,... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 REDUCE WEIGHT FRUTA PLANTA Capsules, 400 mg, supplied in 30 count boxes, dist... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 Super Fat Burning Bomb Capsules, 400 mg, supplied in 30 count boxes, distribu... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 JIANFEIJINDAN Activity Girl Capsules, 400 mg, supplied in 30 count boxes, dis... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 SlimEasy Herbs Capsule, 400 mg, supplied in 30 count boxes, distributed by My... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 Pill for weight reduction, (Japanese Chinese Formula from Japan Hokkaido Cang... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 Meizi Evolution Soft Gel Capsules, supplied in 30 count bottles, distributed ... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, suppl... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I
Jan 24, 2014 Fruta BIO 400 mg capsules, supplied in 30 count boxes, distributed by MyNicKn... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclare... Class I

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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