{
  "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": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "74057",
      "recalling_firm": "Pharmedium Services, LLC",
      "address_1": "150 N Field Dr Ste 350",
      "address_2": "N/A",
      "postal_code": "60045-2506",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1383-2016",
      "product_description": "10 mcg/mL HYDROmorphone HCl  and 0.0625% Bupivacaine HCl in 0.9% Sodium Chloride, 250 mL in 250 mL Baxter Intravia Bag, Rx Only,  Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-733-17",
      "product_quantity": "55 bags",
      "reason_for_recall": "Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.",
      "recall_initiation_date": "20160505",
      "center_classification_date": "20160716",
      "termination_date": "20180306",
      "report_date": "20160727",
      "code_info": "Lot Number 160470116M , Exp. Date 5/17/2016 ;  Lot Number 160490123M , Exp. Date 5/19/2016 ;  Lot Number 160800048M , Exp. Date 6/18/2016 ;  Lot Number 160890060M , Exp. Date 6/27/2016 ;  Lot Number 160940050M , Exp. Date 7/2/2016 ;",
      "more_code_info": ""
    }
  ]
}