{
  "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": "Utica",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72639",
      "recalling_firm": "PQ Corporation",
      "address_1": "340 E Grove St",
      "address_2": "N/A",
      "postal_code": "61373-9001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Kentucky",
      "recall_number": "D-0564-2016",
      "product_description": "EPSOM SALT(Magnesium Sulfate Heptahydrate, USP), 50 lb multi-wall bag, Rx only, Manufactured by PQ Corporation, P.O. Box 840, Valley Forge, Pennsylvania USA 19482.",
      "product_quantity": "41,650 lbs. (833 bags)",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: Level of iron exceeds the limit set by the USP monograph for it (USP limit is NMT 0.5 ug/g (ppm)).",
      "recall_initiation_date": "20151029",
      "center_classification_date": "20160107",
      "termination_date": "20161221",
      "report_date": "20160113",
      "code_info": "Lot # U150511; Exp. 05/18"
    }
  ]
}