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
- Guidance and FAQs
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
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 - 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.
- Notice of Product Recall - 09/17/24
- Licensee Product Recall List - 09/17/24
- Consumer Recall List - 09/17/24
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.
- Notice of Product Recall - 08/30/24
- Licensee Product Recall List - 08/30/24
- Consumer Recall List - 08/30/24
08/08/2024 - C & C Manufacturing LLC, MAN000105
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.
- Notice of Product Recall - 08/08/24
- Licensee Product Recall List - 08/08/24
- Consumer Recall List - 08/08/24
08/06/2024 - NGWMO, LLC, CUL000069
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.
- Notice of Product Recall - 08/06/24
- Licensee Product Recall List - 08/06/24
- Consumer Recall List - 08/06/24
Archived Product Recalls
08/14/2023 - Delta Extraction, LLC, MAN000022
DCR is issuing a product recall on manufactured products sold to dispensaries and manufacturers by infused product manufacturer, Delta Extraction, LLC, MAN000022.
- Notice of Product Recall – Updated 10/20/23
- Product Recall List – Updated 10/20/23
- Products Removed from Recall List – 10/20/23
- Recalled Product Transfer Request – 11/17/23
- Recalled Product Voluntary Destruction Request – 11/17/23