{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Indianola",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80727",
      "recalling_firm": "Bayer Medical Care, Inc.",
      "address_1": "1 Bayer Dr",
      "address_2": "N/A",
      "postal_code": "15051-9702",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The devices were distributed to the following US states:  OH, TX, and WV.",
      "recall_number": "Z-2960-2018",
      "product_description": "Overhead Counterpoise Systems (OCS), OCS CONF,STD CEIL MNT, STD HORZ ARM, Catalog # OCS 115A, Material Number 59880253",
      "product_quantity": "2",
      "reason_for_recall": "The torque wrench used on the ceiling column assembly during a recent service visit was outside of the torque specification, potentially overtightening the bolts. The overtightening of bolts may compromise the structural integrity of the system which could lead to the OCS disengaging from the ceiling mount and this may cause injury to the patient or the operator.",
      "recall_initiation_date": "20180628",
      "center_classification_date": "20180831",
      "termination_date": "20181126",
      "report_date": "20180912",
      "code_info": "Serial Numbers: 11051103902, 305746202"
    }
  ]
}