Bee Extremely Amazed LLC

Complete recall history across all FDA and CPSC categories — 14 total recalls

Bee Extremely Amazed LLC 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 (14)

FDA drug safety enforcement actions by Bee Extremely Amazed LLC

Date Product Reason Class
Dec 15, 2015 ZI XIU TANG BEAUTY FACE & FIGURE Capsules, 250 mg, 60-count bottles Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Asset extreme+PLUS Capsules, 500 mg, 30-count bottles, Distributed by Descor... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 XCEL Capsules, 300 mg, 60-count bottles, Manufactured for JNS Health Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 EVOLVE BEE POLLEN Capsules, 250mg, 60-count bottles, Manufactured for 2637 E.... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 XCEL ADVANCED Capsules, 350mg, 60-count bottles, Manufactured for JNS Health Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Jenesis Capsules, 350 mg, 60-count bottles, Manufactured for Timeless Soluti... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Infinity Capsules, 500 mg, 30-count bottle, Manufactured for Floyd Nutrition Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 La' Trim Plus Capsules, 350 mg, 60-count bottles, Manufactured for: MWN Heal... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 SLIM TRIM U Capsules, 250mg, 60-count bottles, Manufactured for Floyd Nutrition Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Ultimate Formula Capsules, 250mg, 48-count bottles, Manufactured for: Zi Xiu ... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Oasis Capsules, 500mg, 45-count bottles, Manufactured for: MWN Health 37 N O... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 Asset BOLD Capsules, 500 mg, 60-count bottles, Distributed by Descor, LLC www... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... Class I
Dec 15, 2015 SlimeX-15 Capsules, 15 mg, 30-count bottles, Marketed by: Signature Pharmaceu... Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary ... 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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