{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Clemente",
      "address_1": "951 Calle Amanecer",
      "reason_for_recall": "ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially product sterility.",
      "address_2": "",
      "product_quantity": "300 units",
      "code_info": "Lot No. 2704633, 2705206",
      "center_classification_date": "20140820",
      "distribution_pattern": "Nationwide Distribution - USA including AL and MD.",
      "state": "CA",
      "product_description": "CAP Change Kit w/MicroClave Clear, Item No. B78109    BD prefilled syringes are co-packaged into a kit with ICU devices and other components. The affected lots are easily identifiable via the lot number printed on the pouch.",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ICU Medical, Inc.",
      "recall_number": "Z-2293-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68973",
      "termination_date": "20150226",
      "more_code_info": "",
      "recall_initiation_date": "20140805",
      "postal_code": "92673-6212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}