{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Horsham",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88724",
      "recalling_firm": "Flower Orthopedics Corporation",
      "address_1": "100 Witmer Rd Ste 280",
      "address_2": "",
      "postal_code": "19044-2647",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, CO,CT, FL, IL,  IN,  NC, NY, NV, OH, WV, TX.",
      "recall_number": "Z-0034-2022",
      "product_description": "Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201",
      "product_quantity": "77 kits",
      "reason_for_recall": "Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)",
      "recall_initiation_date": "20210903",
      "center_classification_date": "20211006",
      "termination_date": "20220728",
      "report_date": "20211013",
      "code_info": "Lot Number:  2104321637 Unique Identifier: 00840118112079",
      "more_code_info": ""
    }
  ]
}