{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Skaneateles Falls",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76552",
      "recalling_firm": "Welch Allyn Inc",
      "address_1": "4341 State Street Rd",
      "address_2": "N/A",
      "postal_code": "13153-5300",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) Distribution",
      "recall_number": "Z-1777-2017",
      "product_description": "Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch Allyn Inc., 4341 State Street Road, Skaneateles Falls, NY 13153 --- Microlife Corporation 9F, 431, RuiGuang Road, NeiHu, Taipei, 11492, Taiwan, R.O.C. --- Microlife AG Espenstrasse 139 9443 Widnau, Switzerland",
      "product_quantity": "981 units",
      "reason_for_recall": "A defective electrical component in the battery charging circuit in two lots of the ProBP 2400 may potentially cause an over-voltage battery charging condition when the device is connected to the external power supply/battery charger. This potential defect resides with the device, not the battery.  The over-voltage condition can result in high NiMH battery temperatures that, in some cases, can reach levels sufficient to cause melting of the plastic battery door and other adjacent plastic and foam device components.",
      "recall_initiation_date": "20170227",
      "center_classification_date": "20170411",
      "termination_date": "20190614",
      "report_date": "20170419",
      "code_info": "Lot Number 0715:  Serial Number range (21)07150001 - \u0013 (21)07150620; Lot Number 1215: Serial Number range (21)12150001 - \u0013 (21)12150500;  --- Note: (21) is NOT part of the serial number.  It is the Global Unique Device Identification (GUDI) Application Identifier that precedes the serial number on any GUDI compliant label.",
      "more_code_info": ""
    }
  ]
}