{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "275 N Field Dr",
      "reason_for_recall": "Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this malfunction occurs, the pump will alarm and infusion stops.",
      "address_2": "",
      "product_quantity": "69",
      "code_info": "Serial Number  12921204   12922976   12924008   12925861   12925924   12925998   12928528   12928807   12929016   12929126   12920432   12920820   12920856   12920915   12921404   12921413   12922304   12922976   12925861   12925998   12927215   12929016   12931044   12931141   12931155   12931192   12931244   12931342   12931361   12931413   12931610   12931639   12931649   12931911   12921480   12921487   12923723   12924326   12924350   12924546   12925259   12925447   12926315   12927938   12928075   12928614   12930418   12930709   12930890   12931441   12931760   12931911   12932487   12932717   12920754   12920791   12920897   12921063   12921613   12922062   12923441   12924161   12926859   12927756   12928775   12929346   12929438   12931942   12920112",
      "center_classification_date": "20160922",
      "distribution_pattern": "United States (Nationwide) Distribution including Puerto Rico and American Virgin Islands.",
      "state": "IL",
      "product_description": "LifeCare PCA 3, PCA Serial List Number 12384    Allows for clinician administration or self-administration of analgesic medications.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "Z-2874-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "64230",
      "termination_date": "20161107",
      "more_code_info": "",
      "recall_initiation_date": "20130308",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}