{
  "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": [
    {
      "status": "Completed",
      "city": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90542",
      "recalling_firm": "SAFE ORTHOPAEDICS LLC",
      "address_1": "700 W Irving Park Rd",
      "address_2": "",
      "postal_code": "60613-1170",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to MD.  There was no government/military distribution.",
      "recall_number": "Z-1572-2022",
      "product_description": "SteriSpine PS kit of 2 Multi-Axial Fenestrated Screws, model numbers/REF numbers   KITM640, KITM645, and KITM740.",
      "product_quantity": "8 devices",
      "reason_for_recall": "The type of screw printed on the traceability record for the patient label is incorrect, but the type of screw printed on the other labeling is correct.",
      "recall_initiation_date": "20220603",
      "center_classification_date": "20220824",
      "report_date": "20220831",
      "code_info": "KITM640:  Lot numbers BF0A07 and 15BF001/R10; UDI 03760219910053;  KITM645:  Lot number BG0A02; UDI 03760219910060; and  KITM740:  Lot number BL0A01; UDI 03760219910091.",
      "more_code_info": ""
    }
  ]
}