{
  "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": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes",
      "address_2": "",
      "product_quantity": "4,200 containers",
      "code_info": "Lot C931923, exp 8/31/2015",
      "center_classification_date": "20140821",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015",
      "report_date": "20140827",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "D-1550-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "68089",
      "termination_date": "20150629",
      "more_code_info": "",
      "recall_initiation_date": "20140512",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}