{
  "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": "Arcadia",
      "address_1": "5635 Peck Rd",
      "reason_for_recall": "The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900, that did not meet the required specifications for tensile strength. Failure of these rivets could allow the cuff to become disconnected from the connecting strap and allow patients to regain free use of the limb.",
      "address_2": "",
      "product_quantity": "1673 units",
      "code_info": "The model/catalog number for the device is 2900. All lots are being recalled.",
      "center_classification_date": "20130409",
      "distribution_pattern": "Nationwide Distribution",
      "state": "CA",
      "product_description": "Posey Biothane Restraint Cuffs, Catalog Number 2900.    The device is intended to limit a patient's movement to the extent necessary for treatment or protection of the patient or others.",
      "report_date": "20130417",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "J T Posey Company",
      "recall_number": "Z-1071-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63622",
      "termination_date": "20140717",
      "more_code_info": "",
      "recall_initiation_date": "20121031",
      "postal_code": "91006-5851",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}