{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89117",
      "recalling_firm": "Medshape, INC.",
      "address_1": "1575 Northside Dr Nw Ste 440",
      "address_2": "N/A",
      "postal_code": "30318-4211",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Domestic: CA, FL, GA, IL, IN, MA, MD, TX, and WA.",
      "recall_number": "Z-0453-2022",
      "product_description": "DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile",
      "product_quantity": "26 units (1 count)",
      "reason_for_recall": "The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.",
      "recall_initiation_date": "20211117",
      "center_classification_date": "20220104",
      "report_date": "20220112",
      "code_info": "Model No. 2600-05-006; Lot No. 04882; UDI: M97026000500060"
    }
  ]
}