{
  "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": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65420",
      "recalling_firm": "Codman & Shurtleff, Inc.",
      "address_1": "325 Paramount Drive",
      "address_2": "N/A",
      "postal_code": "02767",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of FL, NC, NJ, and TX, and the countries of Austria, Belgium, Spain, Great Britain, Germany, Italy, Ireland, Luxemburg, Russia, Saudi Arabia, Portugal, Greece, Egypt, Switzerland, and Turkey.",
      "recall_number": "Z-1690-2013",
      "product_description": "MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine  Product Code:91-4200 (20ml pump) US 91-4200.    Intended for the intrathecal delivery of Baclofen or Morphine.",
      "product_quantity": "2  units US and 735 OUS",
      "reason_for_recall": "Miscalibrated Fill Level Sensor may affect dosing level",
      "recall_initiation_date": "20130607",
      "center_classification_date": "20130716",
      "termination_date": "20150421",
      "report_date": "20130724",
      "code_info": "All serial numbers"
    }
  ]
}