{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90239",
      "recalling_firm": "Teva Pharmaceuticals USA Inc",
      "address_1": "400 Interpace Pkwy Bldg A",
      "address_2": "",
      "postal_code": "07054-1120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed nationwide in the US Market",
      "recall_number": "D-0988-2022",
      "product_description": "Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-1501-02, Distributed by: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054,  Vial NDC 0703-1501-01",
      "product_quantity": "3109 cartons",
      "reason_for_recall": "Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing",
      "recall_initiation_date": "20220518",
      "center_classification_date": "20220607",
      "termination_date": "20231208",
      "report_date": "20220615",
      "code_info": "Lot #:100022404, Exp Date 10/2022; Lot #:100023333, Exp Dat 12/2022",
      "more_code_info": ""
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}