{
  "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": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "800 MacArthur Blvd.",
      "reason_for_recall": "Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.",
      "address_2": "",
      "product_quantity": "13 units",
      "code_info": "p/n 9201F-PA000XX    DS-    0C000565  02000335  12000603  12000599  12000597  OCOOO569  9A000247  9A000252  17000648  06000490  05000470  05000466  02000373",
      "center_classification_date": "20130127",
      "distribution_pattern": "US Nationwide Distribution including the states of: VA, TN, FL, & TX",
      "state": "NJ",
      "product_description": "Mindray  DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.",
      "report_date": "20130206",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mindray DS USA, Inc. d.b.a. Mindray North America",
      "recall_number": "Z-0742-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63800",
      "termination_date": "20131022",
      "more_code_info": "",
      "recall_initiation_date": "20120905",
      "postal_code": "07430",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}