Qtrade Teas And Herb

Complete recall history across all FDA and CPSC categories — 6 total recalls

Qtrade Teas And Herb 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.

Food Recalls (6)

FDA food safety enforcement actions by Qtrade Teas And Herb

Date Product Reason Class
Apr 22, 2016 Organic Ginger Root Tea Bag Cut (TBC), 25 kgs QTrade Teas & Herbs is recalling Organic Ginger Root Tea Bag Cut (TBC) becaus... Class II
Apr 22, 2016 Organic Ginger Peach Iced Tea, 100x1oz box, item #60001 QTrade Teas & Herbs is recalling Organic Ginger Root Tea Bag Cut (TBC) becaus... Class II
Apr 22, 2016 Organic Coconut Chai Tea Bag Cut (TBC), Net: 25kg QTrade Teas & Herbs is recalling Organic Ginger Root Tea Bag Cut (TBC) becaus... Class II
Apr 22, 2016 Organic Green Tea Hojicha, Net 16 kgs, (bulk product 16 kg boxes with inner... QTrade Teas & Herbs is recalling Organic Green Tea Hojicha because it has th... Class II
Apr 11, 2016 Organic Chamomile Tea Bag Cut (TBC) bulk sold in original cases (25kg bags), ... QTrade Teas & Herbs is recalling Organic Chamomile Tea Bag Cut (TBC) because ... Class II
Feb 8, 2013 Organic Lemon Grass Tea Bag Cut (TBC), Item#410. Packing Size: 25 kgs net... QTrade Teas & Herbs is recalling Organic Lemon Grass Tea Bag Cut (TBC) becaus... 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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