{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88890",
      "recalling_firm": "OmniLife Science",
      "address_1": "480 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to states of: Colorado and Virginia.",
      "recall_number": "Z-0237-2022",
      "product_description": "OMNI K2 Hip Stem, Manufacturer's Product Code 130006  The OMNI K2 Hip Stem is intended for use as the femoral component of a primary total hip replacement. This femoral hip stem is intended for uncemented fixation and single use implantation.",
      "product_quantity": "7",
      "reason_for_recall": "The device is missing grit blasting on the proximal surface of the femoral stem, which may lead to the possibility of product revision in the event of undersizing.",
      "recall_initiation_date": "20211001",
      "center_classification_date": "20211116",
      "termination_date": "20220720",
      "report_date": "20211124",
      "code_info": "UDI 00841690102496  Lot 38933",
      "more_code_info": ""
    }
  ]
}