Bethel Nutritional Consulting, Inc

Complete recall history across all FDA and CPSC categories — 5 total recalls

Bethel Nutritional Consulting, 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 (5)

FDA drug safety enforcement actions by Bethel Nutritional Consulting, Inc

Date Product Reason Class
Dec 19, 2014 B-Lipo, 30 Capsules, Manufactured by KM DALI, Kunming, China for Bethel Nutri... Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a control... Class II
Dec 19, 2014 SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc. Marketed Without An Approved NDA/ANDA: Product was found to contain sibutrami... Class I
Aug 5, 2013 Quick Thin (citrus aurantium extract, sweet potato fiber, cyamopsis gum powde... Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of ... Class I
Aug 5, 2013 Bethel Advance (bitter orange, mulberry leaf, cassia seed extract, jobstear s... Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of ... Class I
Jun 11, 2013 Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. ... Marketed Without An Approved NDA/ANDA: FDA analysis found this product contai... 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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