{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "140480",
      "product_res_number": "Z-0341-2016",
      "event_date_initiated": "2015-09-03",
      "event_date_posted": "2015-11-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2017-11-30",
      "res_event_number": "72288",
      "product_code": "NJT",
      "product_description": "Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10). Immunohistochemistry. in vitro diagnostic.    0.1ml NCL-CD10-270 and 1mL NCL-CD10-270 are intended for the qualitative identification by light microscopy of CD10 molecules in paraffin sections.",
      "code_info": "CD10-270-CE-S (0.1 ml) 6033086 (U.S. Distribution) expire 06/2016, 6032390 expires 04/2016, 6033622 expires 07/2016.   CD10-270-CE (1ml) 6032742 (U.S. Distribution) expires 11/2017.",
      "firm_fei_number": "3000210133",
      "recalling_firm": "Leica Microsystems, Inc.",
      "address_1": "1700 Leider Ln",
      "city": "Buffalo Grove",
      "state": "IL",
      "postal_code": "60089-6622",
      "additional_info_contact": "Katya McGee\n800-225-8867",
      "reason_for_recall": "These Lot numbers are not stable up to the expiry date on the product labeling.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Leica sent a MEDICAL DEVICE RECALL NOTIFICATION letter dated September 3, 2015 via mail to all of the consignees. The letter identified the affected, product, problem and actions to be taken.  Customers are instructed to discontinue use of the reagent lots listed in the recall notification.  It is requested that customers appropriately destroy any unused or partially used affected lots of the reagent, and indicate on the attached Medical Device Recall Notification Acknowledgement Form that this action has been undertaken. Customers were asked to confirm receipt of the notice as soon as possible by signing and dating the attached Medical Device Recall Notification Acknowledgement Form and fax it back to1-847-236-3747, to receive your\nalternative replacement for applicable orders.  For questions contact your local Leica representative.",
      "product_quantity": "U.S: 1 unit of CD10-270-CE-S & 66 units of CD10-270-CE. Foreign: 83 units of CD10-270-CE-S & 219 units of CD10-270-CE",
      "distribution_pattern": "Worldwide Distribution - US Nationwide, Australia, Austria, Brazil, Canada, China, Czech Republic, Finland, France, Germany, Hungary, Indonesia, Ireland, Israel, Italy, Japan, Netherlands, Norway, Romania, Singapore, Slovenia, South Korea, Spain, Sweden, Switzerland and UK.",
      "openfda": {
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        ],
        "device_name": "Immunohistochemistry Reagents And Kits",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.1860",
        "device_class": "1"
      }
    }
  ]
}