{
  "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": "all kits 33, 543",
      "code_info": "Pump Part 510180, Lot 11-100453 to 12-101003 found in:   Go Pump Kit 510201-BP. Lot 12-100108 to 12-101538   Go Pump Kit 510349-BP. Lot 12-100935  Go Pump Kit 510642, Lot 12-100616 to 13-100590",
      "center_classification_date": "20130606",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "IN",
      "product_description": "Part 510180 Disposable Single Infusion Pump, ... Elastomeric Pump 300 mL,  2mL/hr,...  found in : GoPump Kit 510201-BP, 5 fenestrated catheter & BIOPATCH;   Go Pump Kit 510349-BP, Epidural Catheter, BioPatch;   Go Pump Kit 510642   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. The medication is delivered via tubing to the surgical site at a very slow rate",
      "report_date": "20130612",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Symbios Medical Products, LLC",
      "recall_number": "Z-1454-2013",
      "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"
    }
  ]
}