{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "27513",
      "product_res_number": "Z-0904-03",
      "event_date_initiated": "2003-05-02",
      "event_date_posted": "2003-06-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-11-03",
      "res_event_number": "26327",
      "product_code": "MGR",
      "pma_numbers": [
        "P000036"
      ],
      "product_description": "Dermagraft, Human Fibroblast -Derived Dermal Substitute, 2 in. by 3 in..",
      "code_info": "Lot 116098",
      "firm_fei_number": "1000148471",
      "recalling_firm": "Smith and Nephew Wound Management (La Jolla)",
      "address_1": "10933 N Torrey Pines Road",
      "address_2": "Ste 200",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92037",
      "additional_info_contact": "Dionicia B. Reblando\n858-754-3700",
      "reason_for_recall": "Did not meet finished device specifications for the DNA criteria.",
      "root_cause_description": "Other",
      "action": "Recall was by telephone on or about May 2, 2003 and by letter on May 7, 2003. Product is to be returned.",
      "product_quantity": "22",
      "distribution_pattern": "To hospitals nationwide.",
      "openfda": {
        "pma_number": [
          "P900033",
          "P960007",
          "P950032",
          "P010016",
          "P000036"
        ],
        "registration_number": [
          "1221816",
          "3003418325",
          "3009882464",
          "3008087383",
          "2029275",
          "1121308"
        ],
        "fei_number": [
          "1000306431",
          "1000148471",
          "3003418325",
          "3009882464",
          "3008087383",
          "1121308"
        ],
        "device_name": "Dressing, Wound And Burn, Interactive",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}