WHY IT MATTERS: Patients and adult consumers purchasing cannabis from licensed New York dispensaries should check current recall lists and verify with their dispensary that any products they have recently purchased or plan to purchase have not been flagged for removal. CLINICAL OVERVIEW: Product recalls in regulated cannabis markets typically arise when testing laboratories identify contaminants such as pesticides, heavy metals, microbial agents, or inaccurate potency labeling that fall outside state-mandated safety thresholds. When a testing facility’s results are called into question or when products are found to be non-compliant, state regulators are obligated to pull those items from dispensary shelves to protect consumers.
OCM issues precautionary recall for select cannabis products tested by Keystone Lab – CBS 6 Albany
WHY IT MATTERS: Patients relying on tested and labeled cannabis products from New York dispensaries should check the OCM recall list to confirm their specific products are safe to use and return any flagged items to their point of purchase. CLINICAL OVERVIEW: Regulatory bodies like the New York State Office of Cannabis Management have the authority to issue precautionary recalls when questions arise about the accuracy or integrity of third-party laboratory testing, which serves as the primary safety checkpoint between cultivators and consumers. Cannabis testing laboratories are responsible for verifying potency, pesticide levels, heavy metals, residual solvents, and microbial contamination, and any uncertainty in those results can expose patients and consumers to unquantified risks.