{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Bend",
      "address_1": "340 Sw Columbia St",
      "reason_for_recall": "Non-sterile product was shipped to customers labelled as sterile.",
      "address_2": "",
      "product_quantity": "81 units",
      "code_info": "Lot Number L-008926-16037  Lot numbers L-008918-16048, and L-008918-16045   Lot numbers L-008936-16275, and L-008933-16078",
      "center_classification_date": "20210302",
      "distribution_pattern": "US Nationwide distribution in the states of CA, NJ and OR.",
      "state": "OR",
      "product_description": "Various reprocessed products:   PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO;   PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg;  PROVISION Reprocessed Smith and Nephew Trocars/ Cannulas (Class I);  PROVISION Reprocessed Conmed/ Linvatec Suture Retrievers/ Passers C6387  See updated product list attached for details.",
      "report_date": "20210310",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ReNovo, Inc.",
      "recall_number": "Z-1159-2021",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "87258",
      "more_code_info": "",
      "recall_initiation_date": "20210119",
      "postal_code": "97702-1035",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}