{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "114273",
      "product_res_number": "Z-0337-2013",
      "event_date_initiated": "2012-10-24",
      "event_date_posted": "2012-11-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-02-06",
      "res_event_number": "63581",
      "product_code": "LMF",
      "pma_numbers": [
        "P810040"
      ],
      "product_description": "Superstat Modified Collagen Hemostatic Sponge, 2x2 Pledget, 3.0%, Part# 9106-00.\n \nFor use when hemostasis is desired along suture lines, in diffusely bleeding sites, in incisions, dissections, and around arterial or venous anastomoses. Indicated in oozing bleeding, either capillary or venous, in almost all types of incisions or wounds, and as an adjunct to conventional closure techniques",
      "code_info": "Lot# SSF02, SSF03.",
      "firm_fei_number": "3001452136",
      "recalling_firm": "Superstat Corp",
      "address_1": "2015 E University Dr",
      "city": "Rancho Dominguez",
      "state": "CA",
      "postal_code": "90220-6411",
      "additional_info_contact": "310-605-1655",
      "reason_for_recall": "The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.",
      "root_cause_description": "Process control",
      "action": "Superstat initially contacted customers by telephone and sent an Urgent - Device Recall Notification Letter on October 24, 2012, to all affected customers.  The recall letter provided the reason for recall was due to inadequate documentation of quarterly dose sterility audits.  The recall includes all lots and part numbers of Superstat produced between 2002 and 2012.  Customers are instructed to complete and return the enclosed response form as soon as possible.  Customers with questions are instructed to call customer service at (800) 487-3786.\nFor questions regarding this recall call 310-605-1655.",
      "product_quantity": "26,422 units",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of  Saudi Arabia, Thailand, Mexico, Canada, Pakistan,  Israel, Greece,  Serbia, Canda, Isle of Man, Nova Scotia, and Singapore.",
      "openfda": {
        "pma_number": [
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          "P990009",
          "P930030",
          "N17600",
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          "P990030",
          "P810006",
          "P850023",
          "P990004",
          "P050044",
          "P850010",
          "N18286",
          "P830079"
        ],
        "registration_number": [
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        "fei_number": [
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          "3006405073",
          "3035387162"
        ],
        "device_name": "Agent, Absorbable Hemostatic, Collagen Based",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4490",
        "device_class": "3"
      }
    }
  ]
}