{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fountain Valley",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87773",
      "recalling_firm": "STEP-HAR MEDICAL LLC",
      "address_1": "11237 Slater Ave",
      "address_2": "",
      "postal_code": "92708-5417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "IA",
      "recall_number": "Z-1543-2021",
      "product_description": "Alaris Pump Module, Model 8100, serviced/repaired by Step-Har Medical with an impacted bezel repair part",
      "product_quantity": "2",
      "reason_for_recall": "Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.",
      "recall_initiation_date": "20210226",
      "center_classification_date": "20210510",
      "termination_date": "20240815",
      "report_date": "20210519",
      "code_info": "Serial Numbers: 12747983 and 9919591",
      "more_code_info": ""
    }
  ]
}