{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26478",
      "product_res_number": "Z-0708-03",
      "event_date_initiated": "2003-02-25",
      "event_date_posted": "2003-04-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-07-07",
      "res_event_number": "25788",
      "product_code": "MNV",
      "product_description": "DeRoyal''s SurgiMate (tm) Skin Stapler, Rotating Head, product #25-1001, packaged with 35 or more stainless steel staples in peel away pouch. Pouch is labeled in part, ***sterile, disposable, do not resterilize***. Pouches are packaged 12 per box.",
      "code_info": "Finished device lot numbers 502974, 505303, on outside of box. Individual pouches labeled with ''raw'' lot number NH030123-1.",
      "firm_fei_number": "1046367",
      "recalling_firm": "Deroyal Surgical -Rose Hill",
      "address_1": "100 Rose Hill Industrial Park",
      "city": "Rose Hill",
      "state": "VA",
      "postal_code": "24281",
      "additional_info_contact": "Sharon Cook\n888-938-7828 Ext. 6157",
      "reason_for_recall": "Non-sterile surgical medical device is labeled as sterile product.",
      "root_cause_description": "Other",
      "action": "Recalling firm notified consignees by certified mail 2/25/03 and advised to immediately cease using or distributing product. Distributors were requested to further notify their consignees or provide customer contacts. Consignees requested to return response form for replacement product.",
      "product_quantity": "216 units",
      "distribution_pattern": "Product was sold to distributors and direct accounts in PA, TX, WA, AR, HI, CA and TN.",
      "openfda": {
        "device_name": "Strip, Dialysate Ph Indicator",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5820",
        "device_class": "2",
        "registration_number": [
          "2028411",
          "1833387"
        ],
        "fei_number": [
          "1833387",
          "1000125241"
        ],
        "k_number": [
          "K945491",
          "K031267",
          "K941599",
          "K101750",
          "K936311",
          "K944051"
        ]
      }
    }
  ]
}