RecallHawk

doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils

doTERRA International LLC, of Pleasant Grove, Utah

Summary

CPSC recall: doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils. By doTERRA International LLC, of Pleasant Grove, Utah. Hazard: The products contain the substance methyl salicylate, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are applied to the skin or swallowed by young children.. Remedy: Consumers should immediately store the pr

Details

Source

CPSC Consumer Product Recall

External ID

9028

Action Date

2021-04-01

Status

Recalled

Category

consumer_product

Product Description

This recall involves doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerb

Context & Analysis

This is a unclassified recall.

This was one of 5 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

doTERRA International LLC, of Pleasant Grove, Utah has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (doTERRA International LLC, of Pleasant Grove, Utah) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does doTERRA International LLC, of Pleasant Grove, Utah have FDA actions?

doTERRA International LLC, of Pleasant Grove, Utah has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9028" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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