{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90738",
      "recalling_firm": "OrthoPediatrics Corp",
      "address_1": "2850 Frontier Dr",
      "address_2": "N/A",
      "postal_code": "46582-7001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US Nationwide Distribution: AZ, AL, CA, FL, FL, MD, MO, NC, NY, TX   Foreign: Australia",
      "recall_number": "Z-1678-2022",
      "product_description": "Orthex External Fixation  Wire Sharp Bayonet 1.8 x 400 mm  Model:  K400-18BN",
      "product_quantity": "640 units",
      "reason_for_recall": "Manufacturing variance near transition of tip is increasing the likelihood the wire tip may fracture. The fractured tip may be retained in the patient. Retrieval attempts may be made which could result in a delay of surgery and potentially damage soft tissue and increase healing time",
      "recall_initiation_date": "20220629",
      "center_classification_date": "20220906",
      "report_date": "20220914",
      "code_info": "UDI: 00841132179468 Lot Numbers: 239006-B and 238997-B"
    }
  ]
}