{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "219141",
      "product_res_number": "Z-1810-2026",
      "event_date_initiated": "2026-03-12",
      "event_date_posted": "2026-04-10",
      "recall_status": "Open, Classified",
      "res_event_number": "98594",
      "product_code": "QHE",
      "k_numbers": [
        "K241470"
      ],
      "product_description": "LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.",
      "code_info": "Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.",
      "firm_fei_number": "3006721341",
      "recalling_firm": "Linkbio Corp.",
      "address_1": "101 Round Hill Dr Ste 7 101 Round Hill Dr",
      "address_2": "Ste 7",
      "city": "Rockaway",
      "state": "NJ",
      "postal_code": "07866-1214",
      "additional_info_contact": "Jennifer Lubrecht\n973-625-0766",
      "reason_for_recall": "The CORE Workstation may display an incorrect \"Planning Date \" when viewing cases on the \"Start Case\" menu screen.",
      "root_cause_description": "Under Investigation by firm",
      "action": "LinkBio notified consignees on about 03/12/2026 via email. Consignees were instructed to take note of the potential inaccuracy of the \"Planning Date,\" that no product was required to be returned, and to complete and return the Distributor Reply form. LinkBio Corp. is investigating the root cause of the time/date sync issue and will take appropriate action to ensure accurate dates are displayed for the user.",
      "product_quantity": "5 units",
      "distribution_pattern": "US Nationwide distribution  in the state of Alabama, Florida, and Kansas.",
      "openfda": {
        "k_number": [
          "K243509",
          "K241143",
          "K230904",
          "K220452",
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          "K222405",
          "K202151",
          "K261510",
          "K230315",
          "K192074",
          "K241470",
          "K212569",
          "K202454",
          "K200615",
          "K260104"
        ],
        "registration_number": [
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          "3011724582",
          "3015231789",
          "3013561205",
          "3004983210",
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        ],
        "fei_number": [
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          "3011724582",
          "3015231789",
          "3000718467",
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          "3003998208",
          "3014027736",
          "3003714383",
          "3020704423"
        ],
        "device_name": "Shoulder Arthroplasty Implantation System",
        "medical_specialty_description": "Orthopedic",
        "regulation_number": "888.3660",
        "device_class": "2"
      }
    }
  ]
}