{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Peapack",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73285",
      "recalling_firm": "Pfizer Inc",
      "address_1": "100 North Route 206",
      "address_2": "N/A",
      "postal_code": "07977",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0800-2016",
      "product_description": "Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ 07940, NDC 0031-8736-18",
      "product_quantity": "63,636 plastic bottles",
      "reason_for_recall": "Labeling: Label Mix-Up",
      "recall_initiation_date": "20160210",
      "center_classification_date": "20160331",
      "termination_date": "20160622",
      "report_date": "20160406",
      "code_info": "Lot #: R29364; Exp. 10/17"
    }
  ]
}