{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum because packaging integrity (sterile barrier) of the packaging type KIT I may potentially be compromised by transportation.",
      "address_2": "",
      "product_quantity": "16992 total",
      "code_info": "Part Number: 390-0305 (Sigmoid Notch Radial Stem, Small) - Lot #'s 18362, 22834401 and 23852901;    Part Number: 390-0307 (Sigmoid Notch Radial Stem, Large) - Lot #'s 18728, 18815, 18816, 18817, 23834501 and 23853001",
      "center_classification_date": "20150820",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "NJ",
      "product_description": "Sigmoid Notch, Radial Plate, Small, Sterile, Do Not Reuse, Rx Only.  Intended for replacement of the distal radio-ulnar joint following ulnar head resection arthroplasty.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "recall_number": "Z-2430-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "71676",
      "termination_date": "20160429",
      "more_code_info": "",
      "recall_initiation_date": "20150624",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}