{
  "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": [
    {
      "country": "United States",
      "city": "Parsippany",
      "address_1": "399 Interpace Pkwy",
      "reason_for_recall": "Labeling: Label Error on Declared Strength; label on outer carton incorrectly states Diphenhydramine 25 mg instead of 12.5 mg. Also, quantity is incorrectly stated as 30 daytime and 30 nighttime instead of 36 daytime and 24 nighttime.",
      "address_2": "",
      "product_quantity": "738 boxes",
      "code_info": "WO00809739, 9/2017",
      "center_classification_date": "20160922",
      "distribution_pattern": "FL, MA and NJ",
      "state": "NJ",
      "product_description": "Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC 63824-207-60",
      "report_date": "20160928",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Reckitt Benckiser LLC",
      "recall_number": "D-1517-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "74965",
      "termination_date": "20180305",
      "more_code_info": "",
      "recall_initiation_date": "20160803",
      "postal_code": "07054-1133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}