{
  "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": "Norwood",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72570",
      "recalling_firm": "Siemens Healthcare Diagnostics Inc",
      "address_1": "2 Edgewater Dr",
      "address_2": "N/A",
      "postal_code": "02062-4637",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide), Algeria, Armenia, Australia, Austria, Bangladesh, Bosnia Herzegovina, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Ireland, Italy, Japan, Libya, Malaysia, Poland, Portugal, Romania, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., and United Kingdom.",
      "recall_number": "Z-0611-2016",
      "product_description": "Siemens Acute Care DDMR TestPak  Catalog Number: CDDMRE  SMN: 10701511    in vitro diagnostic",
      "product_quantity": "2647",
      "reason_for_recall": "Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems",
      "recall_initiation_date": "20151111",
      "center_classification_date": "20160107",
      "termination_date": "20160923",
      "report_date": "20160113",
      "code_info": "Lot Numbers:  405131002, 405173002, 405187002, 405208002, 405229002  405278002, 405292002"
    }
  ]
}