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The Hain Celestial Group, Inc. - Worldwide HQ

Complete recall history across all FDA and CPSC categories — 4 total recalls

Recall Summary

2 Food Recalls 2 Drug Recalls

The Hain Celestial Group, Inc. - Worldwide HQ appears in recall records across 2 categories. 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 (2)

FDA food safety enforcement actions by The Hain Celestial Group, Inc. - Worldwide HQ

Date Product Reason Class
Dec 7, 2017 BluePrint ORGANIC Beet Blast Vegetable & Fruit Drink 16 fl.oz.(473mL) USDA Or... The label on the back of the bottle may be for the incorrect product. Class III
Jun 3, 2016 MaraNatha¿ All Natural Sunflower Seed Butter, NET WT 12 OZ (340g)., UPC 0 516... A potential for Listeria monocytogenes contamination was verified by the sunf... Class I

Drug Recalls (2)

FDA drug safety enforcement actions by The Hain Celestial Group, Inc. - Worldwide HQ

Date Product Reason Class
Jul 25, 2018 alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g ... Microbial Contamination of a Non-Sterile Product Class II
Jul 5, 2018 alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9... Incorrect Product Formulation: wrong sunscreen product in the package. 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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