{
  "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": "Terminated",
      "city": "Berlin",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89482",
      "recalling_firm": "Merete Medical GmbH",
      "address_1": "Alt-Lankwitz 102",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Domestic: Illinois; Foreign: Germany.",
      "recall_number": "Z-0650-2022",
      "product_description": "Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only",
      "product_quantity": "26 units",
      "reason_for_recall": "Incorrect marketing label (25 mm) was applied to product size 20 mm.",
      "recall_initiation_date": "20220118",
      "center_classification_date": "20220217",
      "termination_date": "20230216",
      "report_date": "20220223",
      "code_info": "Model No. CP20120; Lot No. MS2117816; UDI No. (01)04048266150394(17)260706(10)MS2117816"
    }
  ]
}