{
  "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": "San Jose",
      "address_1": "5900 Optical Ct",
      "reason_for_recall": "Stryker Endoscopy determined that there may not have been adequate determination of required routine checks to ensure accuracy and fitness for use of specific serial numbers of Formula and 180 Shaver Hand Control.",
      "address_2": "",
      "product_quantity": "34 devices",
      "code_info": "Formula Shaver Hand Control, PN 375-704-500 and  Formula 180 (PN 375-708-500).  Serial numbers:  12B037204, 12B037214, 12B037224, 12B037234, 12B040594, 12B040604, 12B040614, 12B040624, 12B040634, 12B040644, 12B040654, 12B040664, 12B040684, 12B041374,  12B046934, 12B046964, 12B046974, 12B046994, 12B047004, 12B047014, 12B047024,  12B047034, 12B047054, 12B047064, 12B047074, 12B047084, 12B047094, 12B049204, 12B049234, 12B049244, 12B055744, 12B055754, 12B055764, 12B055774.",
      "center_classification_date": "20120625",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) including states of: CA, FL, IA , MI, NV, NC, OK, TX, and WI; and countries of: China and Great Britain.",
      "state": "CA",
      "product_description": "Formula Shaver Handpiece (with buttons);  Formula 180 Shaver Handpiece (with button)  Rx only, Made USA.:    Stryker Endoscopy  5900 Optical Court  San Jose, CA 95138    Components within the Crossfire System that provided abrasion, resection, debridement and removal of bone and soft tissue through the Formula Shaver and blade, and the ablation and coagulation of soft tissue, as well as hemostasis of blood vessels through its SERFAS Energy electrosurgical probe.",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Endoscopy",
      "recall_number": "Z-1866-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "61955",
      "termination_date": "20120920",
      "more_code_info": "",
      "recall_initiation_date": "20120521",
      "postal_code": "95138-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}