{
  "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": "2026-08-20",
    "results": {
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  "results": [
    {
      "cfres_id": "176323",
      "product_res_number": "Z-0120-2020",
      "event_date_initiated": "2019-08-28",
      "event_date_created": "2019-10-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-07-23",
      "res_event_number": "83774",
      "product_code": "HFX",
      "k_numbers": [
        "K890897"
      ],
      "product_description": "Centurion  CIRCLAMP W/1.1CM BELL - single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a\nmale infant.\nReOrder: 310CR",
      "code_info": "Batch/Lot:  2019061801",
      "firm_fei_number": "3008403546",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "100 Centurion Way",
      "city": "Williamston",
      "state": "MI",
      "postal_code": "48895-9086",
      "additional_info_contact": "Lisa A. Carpenter\n517-546-5400 Ext. 1156",
      "reason_for_recall": "A  mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.",
      "root_cause_description": "Process control",
      "action": "Centurion Medical Products issued  Notification via Certified Mail, Return Receipt on 8/28/19 to customers who received affected product. Letter states reason for recall, helath risk and action to take: identify inventory within your possession and cease use immediately.  Complete the enclosed accountability record, whether or not you have product, and fax or email at your earliest convenience to the attention of Lisa Carpenter as directed. Upon receipt of  your response  Centurion Representative will contact you regarding retrieval of the product from your facility, if required. Forward this recall information to any facilities to whom this product may have been further distributed, instructing them to cease use immediately. Questions: Kara A. Kowalczy Director of Quality Assurance(517) 546-5400 Ext.1122.\n\nCenturion mailed four (4) additional customer letters on 9/27 /2019 via Certified Mail, Return Receipt.",
      "product_quantity": "1530 each",
      "distribution_pattern": "Nationwide",
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        "device_name": "Clamp, Circumcision",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.4530",
        "device_class": "2"
      }
    }
  ]
}