{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85100",
      "recalling_firm": "Stryker Corporation",
      "address_1": "5900 Optical Ct",
      "address_2": "",
      "postal_code": "95138-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "OUS: Netherlands, Spain, Switzerland, Colombia, Canada, Japan, Taiwan,, Puerto Rico, South Africa, and South Korea",
      "recall_number": "Z-1509-2020",
      "product_description": "Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 07613327051926    This products was distributed with the following sheath/probe:  0250070451-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, Spatula-Tip,  0250070452-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, J-TIP,  0250070453-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, L-TIP,  0250070455-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, Needle Tip",
      "product_quantity": "",
      "reason_for_recall": "Potential diff. in the length of the sheath tube and the sheath/probe. A diff. in length could lead to the base of the sheath/probe not being fully seated in the sheath tube which could result in the distal tip of the sheath melting. This could lead to a compromised insulation, leading to unintentional flow of electricity to the patient.  The sheath/probe is packaged separately.",
      "recall_initiation_date": "20190912",
      "center_classification_date": "20200317",
      "termination_date": "20221031",
      "report_date": "20200325",
      "code_info": "Lot Numbers: 010818-02, 010818-05, 010818-06, 010818-07, 010818-08, 010818-09, 040816-01, 040816-02",
      "more_code_info": ""
    }
  ]
}