{
  "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": "Stockton",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82477",
      "recalling_firm": "Pacific Compounding Pharmacy & Consultations Inc",
      "address_1": "312 Lincoln Ctr",
      "address_2": "N/A",
      "postal_code": "95207-2627",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "California",
      "recall_number": "D-1076-2019",
      "product_description": "Cefuroxime 10mg/mL INJ 0.5 mg, SDV, Rx only, Pacific Compounding, Stockton, CA",
      "product_quantity": "41.4 mL",
      "reason_for_recall": "Presence of Particulate Matter: Particulate matter was reported in one lot of Cefuroxime by a physician after use of product.. FDA analysis identified the particulate as coring of the rubber stopper",
      "recall_initiation_date": "20180823",
      "center_classification_date": "20190402",
      "termination_date": "20230427",
      "report_date": "20190410",
      "code_info": "Lot # 07232018@15 BUD 9/6/18 (frozen)"
    }
  ]
}