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Mary's Medicinal Transdermal Compound Topical

Voluntary recall Label / data Published April 30, 2024

Public-records data from the California Department of Cannabis Control. Original notice on recalls.cannabis.ca.gov.

Recall reason

“Adulterated and Misbranded: Inaccurate Labeling (Cannabinoid inflation)”

The Department of Cannabis Control (DCC) is issuing this notice of voluntary recall for a single Mary's Medicinal Transdermal Compound Topical product(s) due to the presence of Inaccurate Labeling (Cannabinoid inflation). Business Recall Date4/30/2024

DCC verbatim phrases cited on this recall

These are the exact regulator phrases extracted from the DCC reason text on this recall. They are the regulator's words, not editorial summaries.

“cannabinoid inflation” “inaccurate labeling” “misbranded”

Product details

Product type
Topical
Brand
RWC Manufacturing
DCC recall ID
67608862141ebf4b23e92750
Source URL
View on recalls.cannabis.ca.gov →

Licensees implicated

California cannabis recalls frequently name multiple licensees in different roles — the legal business of record (distributor or retailer), the manufacturer that produced the product, and the packager that prepared it for retail sale. All roles published on the DCC portal are reproduced below.

Role Licensee License number License type
Legal Business RWC Manufacturing CDPH-10002341 CDPH Manufacturer
Packaged By rcwmfg.com

Product details

Each row below is a separately-tagged unit on the DCC recall notice. The UID number is the per-unit Metrc tracking tag — the regulator-stamped identifier that follows the unit from cultivation through retail. If you handle California cannabis distribution, you can match these UIDs against your inventory.

Product Batch Size UID Date packaged Date sold
FORMULA 300mg CBG/300 mg CBD/300mg THC 1:1:1 CBG:CBD:THC MFC012424 1oz(28g) 1A4060300001AF7000002257 After February 8, 2024 After February 13, 2024

Locations where this product was sold

Retail licensees that received the recalled product. Each location's license number links to that retailer's full recall history.

ALAMEDA SAN LEANDRO WELLNESS SOLUTIONS INC. C10-0000681-LIC
ALAMEDA EAST BAY THERAPEUTICS C10-0000789-LIC
CONTRA COSTA FIREFLY HEALTH CORPORATION C10-0000667-LIC
EL DORADO KSP99 LLC C10-0000090-LIC
EL DORADO TAHOE GREEN LLC C10-0000751-LIC
EL DORADO CCY CONSULTING INC C10-0000752-LIC
IMPERIAL WINTERHAVEN DRIVE LLC C10-0000906-LIC
KINGS NHC LEMOORE, LLC C10-0000734-LIC
LOS ANGELES THE GREEN GODDESS, INC. C10-0000056-LIC
LOS ANGELES PDLP JV, LLC C10-0001039-LIC
LOS ANGELES THE RESERVE COLLECTIVE COOPERATIVE CORPORATION C10-0001290-LIC
MERCED MERCED BUSINESS VENTURES C10-0000366-LIC
NAPA NAPARC, INC. C10-0001446-LIC
ORANGE WCW ORGANIZATION INC. C10-0000145-LIC
RIVERSIDE THE LEAF AT 73740, LLC C10-0000482-LIC

Showing 1–15 of 42 locations.

Cite this page

Phenominal Consulting. (2026). Mary's Medicinal Transdermal Compound Topical — California cannabis recall, April 30, 2024. Phenominal recall index. Retrieved May 20, 2026, from https://phenominal.io/recalls/67608862141ebf4b23e92750. Underlying data: California Department of Cannabis Control (DCC), recalls.cannabis.ca.gov.

Recall data refreshes daily. When citing this page in a context where the recall classification (Voluntary / Mandatory) or licensee assignment is load-bearing, also reference the authoritative DCC source above.

This page reproduces public-records data from the California Department of Cannabis Control's recall portal at recalls.cannabis.ca.gov. Phenominal Consulting maintains an organized index of the portal, refreshed daily. The underlying recall text is reproduced verbatim from the DCC notice. Category labels (contamination, label/data, mixed, other, packaging) are interpretive groupings applied by Phenominal Consulting based on the DCC reason language; they are not DCC's own classification. For the authoritative version of this recall, refer to the DCC portal. For full methodology and citation format, see the data page.

If your distribution sits on the same data flow

A label-pipeline recall like this is preventable. Most distributors don't know they're exposed.

A 30-minute call to walk through your COA → ERP → label → printer chain — the same pipeline that produced this recall.