{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ra'Anana",
      "state": "N/A",
      "country": "Israel",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81877",
      "recalling_firm": "WEST PHARMA. SERVICES IL, LTD",
      "address_1": "4, Ha-Sheizaf",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distributor in MO",
      "recall_number": "Z-0768-2019",
      "product_description": "Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only",
      "product_quantity": "4.9 million units",
      "reason_for_recall": "Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag is recalled due to similarities with 13mm Vial2Bag DC.",
      "recall_initiation_date": "20181226",
      "center_classification_date": "20190128",
      "termination_date": "20220720",
      "report_date": "20190206",
      "code_info": "UDI:   (01)07290108240047(17)190301(10)7885(90)36098093(91)6070104    Lot Numbers:   7885,  7889,  7889,  8300,  8391,  8646,  8788,  8950,  9038,  9039,  9166,  9167,  9669,  9682,  9982,  A672,  C063,  C070"
    }
  ]
}