{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "West Chester",
      "address_1": "1302 Wrights Ln E",
      "reason_for_recall": "Particle residue on the instrument from adhesive tape which was used to bind the device during transport. There may be a risk of tissue reaction if a patient is exposed to latex particles from the adhesive tape, or a systemic reaction such as anaphylaxis in patients with latex allergy.",
      "address_2": "",
      "product_quantity": "11",
      "code_info": "Radiolucent Retractor for Upper Cervical Spine part number 387.580, lot number 3620715.",
      "center_classification_date": "20141020",
      "distribution_pattern": "US Distribution including the states of  PA, NC, TN, NY, WI, WA and MI.",
      "state": "PA",
      "product_description": "DePuy Synthes Radiolucent Retractor, part number 387.580, lot number 3620715",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes, Inc.",
      "recall_number": "Z-0092-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69432",
      "termination_date": "20151218",
      "more_code_info": "",
      "recall_initiation_date": "20141002",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}