Product Recalls

The Division of Cannabis Regulation (DCR) is committed to ensuring patients and consumers have access to safe cannabis product. Patients and consumers who experience life-threatening reactions to marijuana should seek immediate medical attention. Patients and consumers are reminded that any adverse reactions should be reported to CannabisComplaints@health.mo.gov or fill out a complaint form.

Administrative Holds

Request Documents
- Administrative Hold Review Request (9/20/2024)
- Administrative Hold Review Request – Tag List (9/20/2024)
- Administrative Hold Product Transfer Request (8/21/2024)
- Administrative Hold Product Voluntary Destruction Request (8/21/2024)
Guidance and FAQs
- Retesting of Final Marijuana Product on Administrative Hold Due to Non-Compliant Mandatory Testing (9/20/2024)
- Product Returns and Storage; Products on Administrative Hold FAQ (8/21/2024)

Current Product Recalls

Patients and consumers who have purchased the recalled product should stop using it. All unused product(s) should be discarded or returned to the dispensary where purchased. Returned products will not count toward a patient’s purchase limit. For more information on returns, please contact the dispensary where the product was purchased.

Public Marijuana Product Recalls - 08/16/24

9/16/2026- MAN000103, CCMRB Processing, LLC

DCR in partnership with CCMRB Processing, LLC, is issuing a marijuana product recall on marijuana product M00002615049: Juicy - Juicy J's - Infused Pre Rolls - 2.5g - 5ct. - CHERRY LIMEADE produced by CCMRB Processing, LLC, MAN000103. The recalled marijuana product was tested as part of the routine sampling initiative implemented in July 2025 to ensure safety, label accuracy and consistency with state testing standards. The product did not pass testing for Aspergillus. Aspergillus is a common mold that can be tolerated in small amounts by healthy individuals but may cause adverse health effects in high amounts or in individuals with compromised immune systems.

Notice of Product Recall - 09/16/2026
Licensee and Consumer Product List - 09/16/2026

9/2/2026 - MAN000042, GF Extraction Lab LLC

DCR in partnership with GF Extraction Lab LLC, MAN000042, is issuing an alert to patients and consumers about a mandatory product recall on marijuana products originating from manufacturing licensee GF Extraction Lab LLC, MAN000042. The recalled products contain cannabinoids produced through chemical modification, conversion, or synthetic derivation of cannabinoids.

Notice of Product Recall - 09/02/2026
Licensee and Consumer Product List - 09/02/2026

5/27/2026 – MAN000016, CPC of Missouri – Smithville, LLC

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.

Notice of Product Recall - 05/27/2026

File

Licensee and Consumer Product List - 05.27.2026

5/1/2026 – CUL000053, Sinse Cultivation Cherokee, LLC

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.

Notice of Product Recall - 05/01/2026
File

Licensee and Consumer Product List - 05.01.2026.xlsx

Archived Product Recalls

2025 Recalls

07/01/25 – MAN000030, Bootheel CannaCare Columbia LLC

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.

Notice of Product Recall (07/01/25)
Licensee and Consumer Product Recall List (07/01/25)

04/29/25 – MAN000086, Nodaway Holdings LLC

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.

Notice of Product Recall (04/29/25)
Licensee and Consumer Product Recall List (04/29/25)

04/18/25 – MAN000010, 1913 Carrollton Manufacturing LLC

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.

04/18/25 – MAN000044, Honey Green, LLC

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.

2024 Recalls

11/15/24 – MAN000097, Noah’s Arc Foundation MAN97, LLC

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.

Notice of Product Recall - Updated (11/15/24)
Licensee Product Recall List (11/15/24)
Consumer Recall List (11/15/24)

09/17/24 – TES000007, ClearWater Science, LLC

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.

08/30/24 - MAN000088, Blue Sky Health & Wellness, LLC

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.

08/08/2024 - MAN000105, C & C Manufacturing LLC

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.

08/06/2024 - CUL000069, NGWMO, LLC

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.

2023 Recalls

08/14/2023 - MAN000022, Delta Extraction, LLC

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)

Topic Menu

Administrative Holds

Current Product Recalls

Archived Product Recalls