{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Indianapolis",
      "address_1": "7301 Georgetown Rd.",
      "reason_for_recall": "Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary recall of all GoPumps found in the GoPump Rapid Recovery System kits and all GoBlock kits manufactured with flow control components assembled prior to July 2012. The recall is being expanded after receiving additional reports relating to excessively high flow rates on the 150 mL reservoir, 2 mL/hr GOPump (PN510031), and the",
      "address_2": "Suite 150",
      "product_quantity": "34517 for all kits",
      "code_info": "GoPump Kit 510462-BP, Lot 11-100694- Lot 13-100092  GoPump Kit 510558-BP , Lot 12-100230 - Lot12-101343  GoPump Kit 510643, Lot 12-100332 - Lot 13-100183",
      "center_classification_date": "20130606",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "IN",
      "product_description": "Part510447 Disposable  Infusion Pump, ...Elastomeric  Pump 600 mL,  2mL/hr/side,...  found in the following kits  GoPump Kit 510462-BP, 5 \" catheter & BIOPATCH  GoPump Kit 510558-BP 10 \" catheter& BIOPATCH  GoPump Kit 64310     Disposable Single Infusion Pump. Symbios GOPump Rapid Recovery System is a local pain mangagement system that consists of a small balloon that is inflated with a local anesthetic medication.",
      "report_date": "20130612",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Symbios Medical Products, LLC",
      "recall_number": "Z-1456-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65192",
      "termination_date": "20140307",
      "recall_initiation_date": "20130510",
      "postal_code": "46268",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}