{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Wilmington",
      "address_1": "70 Weil Way",
      "reason_for_recall": "On March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the  traction splint straps. The firm investigated and determined its supplier had labeled the outside packaging for the pediatric and adult traction splints straps incorrectly. The packaging labeled Adult  contained a pediatric splint strap and the packaging labeled pediatric  cont",
      "address_2": "",
      "product_quantity": "153",
      "code_info": "Strap Kit Pediatric Model 443",
      "center_classification_date": "20160504",
      "distribution_pattern": "Worldwide Distribution - US Distribution to the states of : AK ,AZ ,CA, CO, FL ,GA ,HI, IL ,IN ,KY ,MA ,MI ,MS ,NC ,NE ,NJ ,NY ,OH,ON,TX ,VA ,WI , and WV. There are no government accounts for this recall. There is one Canadian account for this recall. There are no Mexican accounts for this recall.  and to the countries of : UAE, MALAYSIA, UNITED KINGDOM, SLOVAKIA, SOUTH AFRICA, QATAR  and AUSTRALIA..",
      "state": "OH",
      "product_description": "Poly-bags containing splint strap labeled with \"Pediatric\" sticker.    Each strap kit contains adjustable length leg straps, ankle wrap, a thigh pad and a heel stand. The strap kits are applied to the traction splint frame to immobilize and provide traction for a patient\u0019s leg.",
      "report_date": "20160511",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ferno-Washington Inc",
      "recall_number": "Z-1603-2016",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "73641",
      "termination_date": "20160823",
      "more_code_info": "",
      "recall_initiation_date": "20160310",
      "postal_code": "45177-9371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}