{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Grand Rapids",
      "state": "MI",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96801",
      "recalling_firm": "SunMed Holdings, LLC",
      "address_1": "2710 Northridge Dr Nw Ste A",
      "address_2": "N/A",
      "postal_code": "49544-9112",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution via Medline.",
      "recall_number": "Z-1814-2025",
      "product_description": "Adult Manual Resuscitator with Medium Adult Mask, Bag REservoir, Filter, Manometer and 7 ft Oxygen Tubing, REF CPRM1116F",
      "product_quantity": "11,358",
      "reason_for_recall": "Affected lots were manufactured with B/V Filter incorrectly attached to the wrong port (patient port instead of the exhalation port). If not noticed prior to patient use, there would be interruption or delay in patient resuscitation, which may lead to life threatening consequences, including hypoxia, hypercapnia, organ failure, and death.",
      "recall_initiation_date": "20250501",
      "center_classification_date": "20250530",
      "report_date": "20250611",
      "code_info": "UDI-DI:  EA: 10884389164822 CS: 40884389164823  Lots: 526782 526790 526796 526797 526798 526800 526802  526804 526805 526806 526807 526808 526809 526810  526814 526815 526816 526811 526817 526818"
    }
  ]
}