{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Montreal",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88396",
      "recalling_firm": "MY01, INC.",
      "address_1": "400 De Maisonneuve Blvd W Suite 700",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MD, OH, CA, NY.",
      "recall_number": "Z-2384-2021",
      "product_description": "MY01 Continuous Compartmental Pressure Monitor, Reference Number MY01-0001",
      "product_quantity": "37 units",
      "reason_for_recall": "There is an incorrect version of the needle in the introducer part of devices. The affected Lots were manufactured using needles with a needle trocar geometry which is out of specification and may require a slightly higher push force from the user to penetrate the patient skin.",
      "recall_initiation_date": "20210628",
      "center_classification_date": "20210827",
      "termination_date": "20220725",
      "report_date": "20210908",
      "code_info": "Lot Numbers:  9448532  9448838  9448979  9449000  9449237"
    }
  ]
}