{
  "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": "Lake Forest",
      "address_1": "275 N Field Dr",
      "reason_for_recall": "Hospira shipped the incorrect replaceable battery pack (Part No: HSP3566-E10) instead of the correct E09 battery pack (Part No. HSP3566-E09) for the Symbiq Single and Dual Channel Infusers.",
      "address_2": "",
      "product_quantity": "59 batteries",
      "code_info": "*** 1) SYMBIQ One-Channel Infuser, List Number: 16026-04-01/02/03/04/25/26/43/44/45/46/51/52/53/54/55/56/57/58/65/66/69/70/77/78/79/80/81/82/83/84/87/88/89/90/93/94;   *** 2) SYMBIQ Two- Channel Infuser, List Number: 16027-04-01/02/03/04/25/26/43/44/45/46/51/52/53/54/55/56/57/58/65/66/69/70/77/78/79/80/81/82/83/84/87/88/89/90/  93/94;    *** X) Battery Pack E10 Part Number: HSP3566-E10;  *** X) Battery Pack E09 Part Number: HSP3566-E09",
      "center_classification_date": "20131120",
      "distribution_pattern": "US Distribution in states of: : KY, MN, ND, NJ, NY, PA, and SD.",
      "state": "IL",
      "product_description": "*** 1) SYMBIQ One-Channel Infuser;   *** 2) SYMBIQ Two-Channel Infuser;    *** E09 batteries can be identified by the \"E09\" that is printed beneath the bar code and at the end of the serial number along the bottom of the label found on each battery;     *** E10 batteries can be identified by the \"E10\" that is printed beneath the bar code and at the end of the serial number along the bottom of the label found on each battery.    Symbiq is a general-purpose infuser designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral, enteral, intra-arterial, subcutaneous, or irrigation routes of administration.",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "Z-0372-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66263",
      "termination_date": "20161107",
      "more_code_info": "",
      "recall_initiation_date": "20130828",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}