Aesop Post-Poo Drops and Aesop Oil Burner Blends
Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia
Summary
CPSC recall: Aesop Post-Poo Drops and Aesop Oil Burner Blends. By Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia. Hazard: The recalled products contain low-viscosity hydrocarbons 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. In addition, the label on the products violates the Federal Hazardous Substances Act (FHSA) by omitting the mandatory info
Details
Source
CPSC Consumer Product Recall
External ID
9359
Action Date
2022-07-28
Status
Recalled
Category
consumer_product
Product Description
This recall involves Aesop Post-Poo Drops, a bathroom deodorizer in a 100 mL amber glass bottle, with a continuous threa
Context & Analysis
This is a unclassified recall.
This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia 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 (Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia have FDA actions?
Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia 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 "9359" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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