Mandatory Recall of GH Kush Pops Medical Cannabis Lollipops for Exceeding THC Limit
Summary
The New Mexico Cannabis Control Division ordered a mandatory recall of GH LLC's "GH Kush Pops" medical cannabis lollipops after finding the product contained 200 mg total THC per package (two 100 mg lollipops), exceeding the state limit of 50 mg THC per serving. Licensed retailers are required to immediately remove the product from shelves. No health-related complaints have been reported.
What changed
The Cannabis Control Division determined that GH LLC's medical cannabis lollipop product exceeded state THC limits, containing 200 mg per package versus the 50 mg legal maximum per serving. The division ordered a mandatory recall, requiring all licensed retailers to immediately remove the product from sale.
Licensed retailers must comply by removing GH Kush Pops from shelves and ensuring no further sales occur. Medical cannabis patients who purchased the product are advised to review product information and contact retailers regarding return or disposal options. Consumers with health concerns should contact the New Mexico Poison and Drug Information Center at 1-800-222-1222.
What to do next
- Licensed retailers must immediately remove GH Kush Pops from shelves
Archived snapshot
Apr 16, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
State recalls medical cannabis edible
Consumer Health and Safety Advisory: State recalls medical cannabis edible
February 26, 2026
SANTA FE –The state has ordered a mandatory recall of a medical cannabis lollipop after regulators found it exceeded the legal THC limit.
The Cannabis Control Division determined that the edible cannabis product, manufactured by GH LLC and sold under the name “GH Kush Pops” contained 200 mg of total THC per package, with two individual 100 mg lollipops. Under New Mexico law, medical cannabis products may contain no more than 50 mg of THC per serving. No health-related complaints have been reported to the division in connection with this recall.
All licensed retailers are required to immediately remove this product from shelves. Full product information, including an example of the product’s packaging and a list of retail locations that received the product, can be found on the division’s website.
Medical cannabis products are reserved for those who hold a medical cannabis ID card issued by the New Mexico Department of Health. Medical patients who purchased this product should review the product information and may contact the retailer for return or disposal options.
Consumption of higher-than-permitted THC levels may increase the risk of adverse effects, including impairment, anxiety, dizziness, rapid heart rate, or other unintended reactions.
Anyone with health-related concerns should contact the New Mexico Poison and Drug Information Center at 1-800-222-1222 or consult their healthcare provider.
Consumers with non-health-related complaints may contact the Cannabis Control Division.
The Cannabis Control Division is committed to protecting public health and safety by ensuring that all cannabis products comply with state regulations. Information about this recall will be posted on the division’s website at: https://www.rld.nm.gov/cannabis/data-news/cannabis-recalls/.
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