{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "190485",
      "product_res_number": "Z-0457-2022",
      "event_date_initiated": "2021-11-19",
      "event_date_created": "2022-01-05",
      "recall_status": "Open, Classified",
      "res_event_number": "89098",
      "product_code": "OOI",
      "product_description": "Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455",
      "code_info": "Kit Product Code MOL1455 (UDI 01-30816101025092) contains 3 discs with Disc Product Code MOL1452. Below lists the MOL1455 Kit Lot numbers (and MOL1452 Disc Lot Numbers):  12410N (12152N), 12411N (12147N), 12413N (12149N), 12477N (12150N), 12602N (11548NA), 12603N (12144N), 12721N (12148N), 12889N (12151N), 13369N (12817N), 13370N (13151N), 13434N (12382N), 13652N (12835N), and 13242N (12154N)*.  *Kit Lot #13242N (Disc Lot #12154N) was shipped to Europe and not within the US.",
      "firm_fei_number": "2023365",
      "recalling_firm": "DiaSorin Molecular LLC",
      "address_1": "11331 Valley View St",
      "city": "Cypress",
      "state": "CA",
      "postal_code": "90630-5366",
      "additional_info_contact": "Ms. Alesia Magon\n651-472-3186",
      "reason_for_recall": "A subset of affected discs are at risk of leakage when it is used more than one time with Simplexa COVID-19 Direct and/or Simplexa Flu A/B & RSV Direct Gen II. Leakage from a well that had a positive sample may cause further cross-contamination in areas of the lab if not properly cleaned.",
      "root_cause_description": "Under Investigation by firm",
      "action": "On 11/19/2021, the firm notified affected customers via email of \"URGENT: MEDICAL DEVICE CORRECTION NOTIFICATION.\" The letter indicated, \"Actions to be taken by the Customer/User/Distributor:\n\n- Any remaining discs in inventory that are listed in the table below should only be used one time and not reused.\n- Any sample with an error code should be retested.\n- If leakage is suspected, the spillage should be removed and the instrument surface should be decontaminated. Ensure the practice of Good Laboratory Procedures including regular cleaning.\n- Notify others within your network that may have received these kits.\n- Complete and return the Acknowledgement and Receipt Form (page 3) of this notification letter.\n- If your firm has further distributed the devices, please share a copy of this correction notification and response form with those customers and provide a copy of the completed response form back to us.\n\nIf you have any questions or if you would like replacement product for the Direct Amplification Discs you still have in stock, please contact DiaSorin Molecular Technical Service, Monday   Friday, 7:00am to 5:00pm (Pacific Time) at (800) 838-4548, option 3, or by email at technicalinfo.molecular@DiaSorin.com.\"",
      "product_quantity": "29495 kits",
      "distribution_pattern": "US:\nAZ,\nCA,\nCO,\nCT,\nDC,\nFL,\nGA,\nHI,\nIA,\nIL,\nIN,\nKS,\nKY,\nLA,\nMA,\nMD,\nME,\nMI,\nMN,\nMO,\nNC,\nND,\nNE,\nNH,\nNJ,\nNM,\nNV,\nNY,\nOH,\nPA,\nRI,\nSC,\nSD,\nTN,\nTX,\nVA,\nVT,\nWA,\nWI,\nWV; and\n\n\nWorldwide:\nKuwait,\nAustralia,\nIsrael,\nItaly,\nCanada,\nChile,\nPuerto Rico,\nUnited Arab Emirates.",
      "openfda": {
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        ],
        "device_name": "Real Time Nucleic Acid Amplification System",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.2570",
        "device_class": "2"
      }
    }
  ]
}