{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Grand Rapids",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80201",
      "recalling_firm": "Sun Med, 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": "IL & OH distributors",
      "recall_number": "Z-2153-2018",
      "product_description": "MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1126C",
      "product_quantity": "113 cases",
      "reason_for_recall": "There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use.  This may impact air delivery to the patient.",
      "recall_initiation_date": "20180524",
      "center_classification_date": "20180609",
      "termination_date": "20200512",
      "report_date": "20180620",
      "code_info": "Lot Numbers: 313321, 313437, 313080 & 313193"
    }
  ]
}