{
  "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,
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  },
  "results": [
    {
      "cfres_id": "113490",
      "product_res_number": "Z-0292-2013",
      "event_date_initiated": "2012-08-21",
      "event_date_posted": "2012-11-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-09-11",
      "res_event_number": "63322",
      "product_code": "LMF",
      "pma_numbers": [
        "P990004"
      ],
      "product_description": "ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin distributed by ETHICON ETHICON Inc. Somerville, NJ  08876 USA  \n\n Ref 2993\n\n\nSURGIFLO Hemostatic Matrix, mixed with sterile saline or thrombin solution, is indicated for surgical procedures (except ophthalmic) for hemostasis, when control of capillary, venous and arteriolar bleeding by pressure, ligature, and other conventional procedures is ineffective or impractical. This is a topical absorbable hemostat consisting of a flowable gelatin matrix (paste) and a lyophilized Thrombin component. This kit also contains components necessary for preparing and applying the matrix during surgery.",
      "code_info": "PMA: P990004 Medical Device Listing Number:  D100622  Product Code 2993  Lot/Batch Numbers:  239346  Exp Jan-13 239411  Exp Jun-13",
      "firm_fei_number": "2210968",
      "recalling_firm": "Ethicon, Inc.",
      "address_1": "US Highway 22 West",
      "city": "Somerville",
      "state": "NJ",
      "postal_code": "08876",
      "additional_info_contact": "877-384-4266",
      "reason_for_recall": "SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with Thrombin have an issue within the packing process where a cut could potentially breach the double Tyvek pouch of the packaging.",
      "root_cause_description": "Packaging",
      "action": "Ethicon Inc. sent an Urgent Product Information letter dated August 21, 2012, to all affected customers.  The letter identified the product, the problem, and the action to be taken by the customer.   Customers were instructed to inspect their inventory to determine if they have any of the affected product.  Affected product should be returned for replacement to Stericycle using the enclosed pre-paid shipping label.    Customers with questions should call 1-877-384-4266 or contact their Ethicon Biosurgery Sales Representative.\nFor questions regarding this recall call 877-384-4266.",
      "product_quantity": "28,276",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of Russia, China, and the European Union.",
      "openfda": {
        "pma_number": [
          "P800002",
          "P990009",
          "P930030",
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          "P810006",
          "P850023",
          "P990004",
          "P050044",
          "P850010",
          "N18286",
          "P830079"
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        ],
        "device_name": "Agent, Absorbable Hemostatic, Collagen Based",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4490",
        "device_class": "3"
      }
    }
  ]
}