{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "150 N Field Dr Ste 350",
      "reason_for_recall": "Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Service Code 2K6127;     15342123S, exp 2/10/2016  15349071S, exp 2/17/2016 and    15351050S, exp 2/19/2016",
      "center_classification_date": "20160317",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61",
      "report_date": "20160323",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Pharmedium Services, LLC",
      "recall_number": "D-0778-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "72973",
      "termination_date": "20160406",
      "more_code_info": "",
      "recall_initiation_date": "20151231",
      "postal_code": "60045-2506",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}