{
  "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": "Branchburg",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63814",
      "recalling_firm": "Roche Molecular Systems, Inc.",
      "address_1": "1080 Us Highway 202 S",
      "address_2": "N/A",
      "postal_code": "08876-3733",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of GA, CA, NC, and MN.",
      "recall_number": "Z-0614-2013",
      "product_description": "COBAS AmpliPrep Instrument (CAP) with AMPLILINK (AL) Software v.3.3.5    Automated sample processing instrument used with CAP/CA and CAP/CTM.    Roche Molecular Systems, Inc.  1080 US Highway 202 South  Branchburg, NJ 08876  USA  Made in Switzerland",
      "product_quantity": "7 units",
      "reason_for_recall": "Certain COBAS AmpliPrep instruments using AMPILINK software v.3.3.4 had the sample clot detection flagging feature disabled during quality control release resulting in samples that may not be flagged as having clots.",
      "recall_initiation_date": "20121011",
      "center_classification_date": "20121222",
      "termination_date": "20130911",
      "report_date": "20130102",
      "code_info": "CAP 394436 to 394663"
    }
  ]
}