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A review of the Pyxis report confirmed that the receipts for the 34 morphine transactions that MEYERS coded as “Surgery” were printed by the machine, but none were forwarded to the Dispensary Technician for billing. MEYERS’ 35th morphine access, conducted on July 8, 2024, was coded under a patient name ("Reggie"). However, based upon a review of “Reggie’s” chart and interviews with “Reggie’s” vet, “Reggie” was never prescribed morphine nor was any administered to “Reggie.” Because MEYERS’ access was coded to “Reggie”, “Reggie’s” bill for services included 1 vial of morphine. “Reggie’s” vet also told police that if “Reggie” had needed morphine, he would have needed 5-6 vials, not just 1. 3 62-CR-26-350 Filed in District Court State of Minnesota 1/16/2026 All other Pyxis transactions that MYERS conducted during the timeframe (accessing drugs other than morphine) were conducted appropriately; they were coded to a specific patient and not “Cancelled.” When the investigation began, the Pyxis machine contained 29 vials of morphine.
All 29 were collected and examined by the FDA. On December 5, 2024, the FDA Forensic Chemistry Center reported that all 29 showed evidence of tampering (puncture wounds on the rubber stopper) and all 29 contained “glue” on the crimp and stopper top. The contents of 7 of the 29 morphine vials were analyzed by the FDA. All 7 were positive for evidence of dilution. Specifically, they contained the following percentages of morphine compared to the label: 5.2%, 13%, 5.8%, 13%, 8.5%, 9.4%, and 3.3%. The FDA also tested a 30th morphine vial that was found in the hospital’s "Waste Bin". It also had “glue” on the crimp and stopper and the remaining liquid in the vial contained only 9.2% of the morphine declared on the label.