Missouri Regulators Issue Recall for Marijuana Vape Products Over Testing Issue

Missouri marijuana regulators have issued a recall for products manufactured by CPC of Missouri – Smithville, LLC, after determining that certain vape products were not tested in accordance with state requirements.

The Missouri Division of Cannabis Regulation announced the recall today in partnership with the company, which operates under manufacturing license MAN000016. Regulators said the recalled products present a potential health and safety concern because the THC concentrates used in the products were tested before being processed into vape cartridges.

Under Missouri rules, THC concentrates must be sampled and tested after being processed into vape cartridges, according to the Division of Cannabis Regulation. The agency said no adverse reactions have been reported to regulators at this time.

Patients and consumers who purchased the recalled products are being told to stop using them immediately. Regulators said unused products should be discarded or returned to the dispensary where they were purchased. Returned products will not count toward a medical marijuana patient’s purchase limit.

Anyone who believes they may be experiencing an adverse reaction should seek immediate medical attention. Regulators also urged patients and consumers to report any adverse reactions by emailing CannabisComplaints@health.mo.gov or by submitting a complaint through the state’s patient, caregiver and consumer complaint process.

A full list of the recalled products is available below and by clicking here.

DCR in partnership with CPC of Missouri – Smithville, LLC is issuing a marijuana product recall on marijuana products sold to dispensary licensees by manufacturing licensee, CPC of Missouri – Smithville, LLC, MAN000016. The recalled products were not tested in accordance with the requirements. For the safety of patients and consumers, DCR testing regulations require that THC concentrates be sampled and tested after being processed into vape cartridges. The testing of the THC concentrates in the recalled products was done prior to being processed into vape cartridges.

DCR in partnership with Sinse Cultivation Cherokee, LLC is issuing a marijuana product recall on marijuana product source tag 1A40C0300000A29000061341sold to dispensary licensees by Cultivation licensee, Sinse Cultivation Cherokee, LLC, CUL000053. The recalled marijuana product was tested and confirmed to contain Pathogenic Aspergillus species detectable in one (1) gram. Aspergillus species in marijuana product presents a potential threat to the health and safety of consumers.

DCR in partnership with Bootheel CannaCare Columbia LLC is issuing a marijuana product recall on marijuana products sold to dispensary licensees by manufacturing licensee, Bootheel CannaCare Columbia LLC, MAN000030. The recalled marijuana products were not compliantly labeled prior to being sold to patients and consumers. The recalled marijuana products contain ingredient (grapefruit mercaptan) not listed on the compliance label as required by 19 CSR 100-1.120(1)(C)2.A. Patients and consumer would not be alerted to its presence. DCR is working with the Licensee to ensure all products not yet sold are compliantly labeled.

DCR is issuing a marijuana product recall on marijuana products sold to dispensary licensees by manufacturing licensee, Nodaway Holdings LLC, MAN000086. The recalled marijuana product design resembles non-marijuana products. In order to protect children and prohibit inadvertent consumption of marijuana products, Department rules prohibit marijuana products from resembling non-marijuana products.

DCR is issuing a product recall on marijuana products sold to dispensary licensees by manufacturing licensee, 1913 Carrollton Manufacturing LLC, MAN000010. The recalled marijuana product packaging and design resembles non-marijuana products. To protect children and prohibit inadvertent consumption of marijuana products, Department rules prohibit marijuana products from resembling non-marijuana products. Additionally, the marijuana product packaging is not the same packaging that was submitted and approved by DCR.

DCR is issuing a product recall on marijuana products sold to dispensary licensees by manufacturing licensee, Honey Green, LLC, MAN000044. The recalled marijuana products were inadvertently labeled with the incorrect product information. Therefore, DCR cannot verify compliance with health and safety requirements.

DCR is issuing a product recall on marijuana products sold to dispensary facilities by comprehensive manufacturing licensee, Noah’s Arc Foundation MAN97, LLC, MAN000097. The recalled marijuana products were not compliantly labeled prior to being sold to patients and consumers. The recalled marijuana product may contain food coloring ingredients not listed on the compliance label as required by 19 CSR 100-1.120(1)(C)2.A.

DCR is issuing a product recall on marijuana products mandatory tested by testing licensee ClearWater Science, LLC, TES000007. The recalled products were not compliantly mandatory tested as mandated by 19 CSR 100-1. Therefore, DCR cannot verify compliance with health and safety requirements.

DCR is issuing a product recall on marijuana products sold to dispensary and manufacturing facilities by comprehensive manufacturing licensee Blue Sky Health & Wellness, LLC, MAN000088. The recalled products were not compliantly tracked in the statewide track and trace system (Metrc) as mandated by 19 CSR 100-1. Therefore, DCR cannot verify compliance with health and safety requirements.

DCR is issuing a product recall on marijuana products sold to dispensary and manufacturing facilities by comprehensive manufacturing licensee C&C Manufacturing, LLC, MAN000105. The recalled products were not compliantly tracked in the statewide track and trace system (Metrc) as mandated by 19 CSR 100-1. Therefore, DCR cannot verify compliance with health and safety requirements.

DCR is issuing a product recall on marijuana products sold to dispensary facilities by comprehensive cultivation licensee, NGWMO, LLC, CUL000069. The recalled marijuana products were not compliantly tested prior to being sold to patients and consumers. The recalled marijuana product was tested at the unprocessed bud/flower stage rather than being tested at the final marijuana product stage as required by 19 CSR 100-1.

DCR is issuing a product recall on manufactured products sold to dispensaries and manufacturers by infused product manufacturer, Delta Extraction, LLC, MAN000022. New marijuana products are identified by an asterisk.

Notice of Product Recall – Updated 06/20/25

Product Recall List – Updated 04/10/25

Products Removed from Recall List – Updated 04/10/25