{
  "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,
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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": "all kits  33,543",
      "code_info": "Pump 510076 Lot 11-100222 to 12-101087 found in:   Kit 510080 BP. Lot 11-100215 to 12-100508  Kit 510141-BP Lot 12-100460 to 12-100673   Kit 510112-BP, Lot 11-100839-to 13-100225",
      "center_classification_date": "20130606",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "IN",
      "product_description": "Part 510076 Disposable Dual Infusion Pump, ...Elastomeric Dual Pump 300 mL(150 ml/side) 2mL/hr/side,... Sterile,  found in the following kits: GoPump kit 510080-BP,  5 fenestrated catheter & BIOPATCH;   GoPump kit 510112-BP,  2.5\" fenestrated catheter & BIOPATCH  Go Pump Kit 510141-BP,10\" fenestrated catheter& BIOPATCH    Disposable Single Infusion Pump for drug delivery 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-1453-2013",
      "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"
    }
  ]
}