{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Mentor",
      "address_1": "5960 Heisley Rd",
      "reason_for_recall": "The Drager Pendula spring arm device has a  set of screws located on the spring arm that were not properly secured with Loctite and may become loose.",
      "address_2": "",
      "product_quantity": "63",
      "code_info": "0419016160  0421416123  0420816119  0415216095  0409016039  0409016038  0404716127  0434815015  0429915001  0429915002  0418015066  0418015065  0416815002  0416015002  0416015001  0413515012  0409615011  0407615001  0407615002  0405015102  0429614003  0401515015  0431714001  0430914002  0430914001  0427614022  0428014006  0423914014  0421714007  0416814001  0415014002  0414314082  0413914001  0412714043  0411414001  0411414003  0411414002  0411114001  0401614001  0404814128  0405014014  0403814116  0402214076  0401314131  0401514013  0400614027  0434413019  0433813017  0429113164  0430113149  0427313064  0417013083  0414813001  0412113002  0412113001  0410013001  0405213038  0404413018  0404413017  0404413016  0404413016  0436112019  0436112018  0434912001",
      "center_classification_date": "20161212",
      "distribution_pattern": "Nationwide Distribution including AK, AZ, CA, CO, FL, IL, KY, MI, MO, NB, NJ, NY, OH, PA, RI, SD, TN, TX, UT, WA & WV.",
      "state": "OH",
      "product_description": "Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS)  The system is intended for use in surgical operating rooms (OR) or intraoperative surgical/imaging rooms where simultaneous multiple image viewing is required",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Steris Corporation",
      "recall_number": "Z-0746-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75385",
      "termination_date": "20170414",
      "more_code_info": "",
      "recall_initiation_date": "20161005",
      "postal_code": "44060-1834",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}