{
  "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": "Philadelphia",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72382",
      "recalling_firm": "Mutual Pharmaceutical Company,  Inc.",
      "address_1": "1100 Orthodox St",
      "address_2": "N/A",
      "postal_code": "19124-3168",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MS",
      "recall_number": "D-0572-2016",
      "product_description": "Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg DOUBLE STRENGTH, 100-count bottle, Rx only, Mfg. by: Mutual Pharmaceutical Company, Inc., Philadelphia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 53489-0146-01",
      "product_quantity": "9526",
      "reason_for_recall": "Presence of foreign substance -This recall has been intiated due to the presence of a polyethylene piece on the finished product.",
      "recall_initiation_date": "20151009",
      "center_classification_date": "20160119",
      "termination_date": "20161013",
      "report_date": "20160127",
      "code_info": "Lot # 6727001 Exp 01/18",
      "more_code_info": ""
    }
  ]
}