The Missouri Division of Cannabis Regulation (DCR) issued a mandatory recall on Aug. 6 for 2,649 products—including flower, pre-rolls and kief—sold to dispensaries by Marceline-based cultivation licensee NGWMO LLC.
The DCR issued the alert to medical cannabis patients and adult-use consumers in cooperation with NGWMO, according to a news release from the Missouri Department of Health and Seniors Services (DHSS).
The recalled cannabis products from this week were not compliantly tested before being sold to patients and consumers, according to the DHSS release.
“The recalled marijuana products were tested at the unprocessed bud/flower stage, rather than being tested at the final marijuana product stage as required by 19 CSR 100-1,” according to the release. “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 facility where purchased.”
The DCR had not received reports of adverse reactions as of Aug. 6, according to the release. Returned products will not count toward a patient’s purchase limit.
The DCR provided a complete list of all 2,649 products, which can be accessed here. All of the products were sold under the Twenty Twenty brand name at 79 of Missouri’s 209 operational dispensaries, according to the recall list.
Additional information on Missouri product recalls is available on the DCR’s website.
