{
  "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": "Cambridge",
      "address_1": "One Kendall Square",
      "reason_for_recall": "Failure of glue joint, allowed a portion of the single use device to shift inside, may separate and fall into the patient",
      "address_2": "Building 100, 3rd floor",
      "product_quantity": "45 units",
      "code_info": "Lot Numbers:  LA121003AO-P1  LA121003AQ-P1  LA121001CB-P1  LA121003AL-P1  LA121002AC-P1  LA121001CC-P1  LA121001BZ-P1  LA121001BZ-P1  LA121001AR-P1  LA121001AQ-P1  LA121001CA-P1  LA120926BA-P1  LA120926AS-P1  LA120919BG-P1  LA120920AF-P1  LA120924AG-P1              :",
      "center_classification_date": "20121203",
      "distribution_pattern": "Nationwide Distribution including AZ, FL, MA,  NY, OH, and OR.",
      "state": "MA",
      "product_description": "OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use  Cat. # BP-ROBOTIC    The OmniGuide Fiber is indicated for the incision, excision, ablation, vaporization and coagulation of body soft tissues including intra-oral tissues. It is indicated in the medical specialties of general and plastic surgery, oral/maxillofacial surgery, dentistry, dermatology, gynecology, otorhinolaryngology, gastroenterology, neurosurgery, urology, and pulmonology, and can be used in open surgical procedures as well as endoscopic minimally invasive procedures in conjunction with rigid or flexible endoscopes, such as in laryngoscopy, gastroscopy, colonoscopy, laparoscopy, thoracoscopy, hysteroscopy and bronchoscopy",
      "report_date": "20121212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "OmniGuide, Inc.",
      "recall_number": "Z-0453-2013",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "63642",
      "termination_date": "20141016",
      "recall_initiation_date": "20121105",
      "postal_code": "02139-1562",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}