{
  "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": "Slany",
      "state": "N/A",
      "country": "Czech Republic",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81927",
      "recalling_firm": "Linet Spol. S.r.o.",
      "address_1": "Zelevcice 5",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL, OK, NJ, OR, WA, CA, MN, LA, AZ, IL, MO, CO, OH, KY, FL, KS, UT, TN, LA, DE, CT, TX",
      "recall_number": "Z-0991-2019",
      "product_description": "AVE 2 Birthing Bed",
      "product_quantity": "253 devices",
      "reason_for_recall": "LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable may fail causing a possible spark or possible exposure to a live conductor.",
      "recall_initiation_date": "20190107",
      "center_classification_date": "20190308",
      "termination_date": "20230531",
      "report_date": "20190320",
      "code_info": "Serial Numbers 4PPB0091 through 4PPB626"
    }
  ]
}