{
  "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": "2026-07-08",
    "results": {
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    {
      "status": "Terminated",
      "city": "West Columbia",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90718",
      "recalling_firm": "Nephron Sterile Compounding Center LLC",
      "address_1": "4500 12th Street Ext",
      "address_2": "",
      "postal_code": "29172-3025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-1347-2022",
      "product_description": "PF-Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL), One 4 mL Unit-Dose Vial, packaged in 30 x 4 mL Sterile Unit-dose Vials per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC 69374-946-34",
      "product_quantity": "33,870 vials",
      "reason_for_recall": "CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.",
      "recall_initiation_date": "20220810",
      "center_classification_date": "20220816",
      "termination_date": "20241011",
      "report_date": "20220824",
      "code_info": "Lot: LB2005A, Exp 3/2/2023",
      "more_code_info": ""
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}