{
  "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": "2026-09-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 3
    }
  },
  "results": [
    {
      "cfres_id": "198226",
      "product_res_number": "Z-1184-2023",
      "event_date_initiated": "2023-01-25",
      "event_date_posted": "2023-02-27",
      "recall_status": "Open, Classified",
      "res_event_number": "91578",
      "product_code": "PBZ",
      "k_numbers": [
        "K142801"
      ],
      "product_description": "Finished Goods Box of 50 Inserts and Scanning Labels for Medivac Guardian 2L\nCatalog Number: FG 12010.\nIntended adjunct in the estimation of blood loss.",
      "code_info": "UDI-DI: 10859506006125\n\nLot Numbers: M2110004, M2201002, M2202001, M2203002, M2206001",
      "firm_fei_number": "3015967359",
      "recalling_firm": "Stryker Corporation",
      "address_1": "1941 Stryker Way",
      "city": "Portage",
      "state": "MI",
      "postal_code": "49002-9711",
      "additional_info_contact": "SAME\n269-800-1941",
      "reason_for_recall": "Triton Canister Software, Insert & Scanning Label\nmay cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result in either delayed recognition or prolongation of postpartum hemorrhage (PPH), or require more aggressive treatment for PPH.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Stryker issued Urgent Medical Device Correction letter to Risk Manager, OR Director, Materials Manager dated Jan 25, 2023. Letter states reason for recall, health risk and action to take:\nSteps:\n1. Immediately check your internal inventory to locate any affected Finished Goods Inserts and Scanning labels (FG 12010 and FG 12022). Quarantine and discontinue use of all affected products.\n2. A Stryker representative will contact your facility to assist updating the Triton Canister software.\n3. Return the enclosed Business Reply Form (BRF) even if you don t have any affected product on hand, via email to instruments.recalls@stryker.com.\n4. If the BRF indicates that recalled product is currently on hand, a shipping label will be provided to return recalled product. Upon receipt of the recalled product, Stryker will arrange replacements.\n5. Maintain awareness of this communication internally until all required actions have been completed within your facility.\n\nContact: Sylvia Page | Stryker Instruments Recall Coordinator 269-501-8375 |Instruments.recalls@stryker.com",
      "product_quantity": "101 units",
      "distribution_pattern": "US Nationwide distribution.",
      "openfda": {
        "k_number": [
          "K252282",
          "DEN130015",
          "K160338",
          "K142801",
          "K232250",
          "K163507"
        ],
        "registration_number": [
          "3010141593",
          "3015967359"
        ],
        "fei_number": [
          "3010141593",
          "3015967359"
        ],
        "device_name": "Image Processing Device For Estimation Of External Blood Loss",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.2750",
        "device_class": "2"
      }
    }
  ]
}