MBi Distributing Inc. dba MBi Nutraceuticals

Complete recall history across all FDA and CPSC categories — 7 total recalls

MBi Distributing Inc. dba MBi Nutraceuticals 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 (7)

FDA drug safety enforcement actions by MBi Distributing Inc. dba MBi Nutraceuticals

Date Product Reason Class
May 15, 2018 Teething Drops, Homeopathic Drops for Temporary Relief of Pain Caused by Teet... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II
May 15, 2018 Silver-Zinc Throat Spray, HOMEOPATHIC IMMUNE DEFENSE, 50PPM, 4oz/50 ppm/ 120m... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II
May 15, 2018 Nausea Drops, Homeopathic Drops for Temporary Relief of Motion Sickness, Morn... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II
May 15, 2018 Expectorant Cough Syrup, Homeopathic Syrup for Temporary Relief of Cough & Br... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II
May 15, 2018 Intestinal Colic Drops, Homeopathic Drops for Temporary Relief of Flatulent C... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II
May 15, 2018 Stomach Calm, Calms Upset Stomach and Aids in Treatment of Simple Diarrhea, ... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II
May 15, 2018 Argentum Elixir Colloidal Silver, 50 PPM Homeopathic Infection Fighter, 8 fl... Lack of Processing Controls: Firm is voluntarily recalling all lots of homeop... Class II

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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