Plant Devas Inc Recall: FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.

🇺🇸 United States

1. February 27, 2018 - Recall initiated
2. March 21, 2018 - Reported by source
3. September 7, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0928-2018

Event ID

79211

Status

Terminated

Classification

Class II

Company

Plant Devas Inc

Product description

Rose Face Care Kit; Each kit contains: Rose Cleansing Milk -- 1 fl oz bottle Rose Geranium Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - ROSE 0.13 fl oz vial Rose Vetiver Day Moisturizer 0.17 fl oz jar French Rose Clay 0.1 oz jar evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Quantity

11,090 units

Reason

FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.

Recall initiation date

February 27, 2018

Report date

March 21, 2018

Classification date

Not published in this source record

Termination date

September 7, 2018

Distribution pattern

One distributor in WI. On line sales nationwide and to Argentina, Australia, Austria, Belgium, Bermuda, Canada, China, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Estonia, Finland, French Polynesia, France, Germany, Greece Hong Kong, India, Indonesia, Ireland, Israel, Italy, Japan, Kuwait, Malaysia. Mexico, Morocco, Netherlands, New Zealand, Nigeria, Norway, Peru, Puerto Rico, Russia, SAR China, Saudi Arabia, Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, UAE,

UPC, lot, and code information

LOT Manuf Date Sell By 7270302 7.3.2017 7.3.2019 7310102 8.1.2017 8.1.2019 7350102 9.1.2017 9.1.2019 7400202 10.2.2017 10.2.2019 7440102 11.1.2017 11.1.2019 7480101 12.1.2017 12.1.2019 8010201 1.2.2018 1.2.2020 8050101 2.1.18-2.12.18 2.1.2020

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 79211 with 7 other product entries in Public Health Trace.

Responsible company: Plant Devas Inc

Other recalls from Plant Devas Inc

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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