{
  "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": "2026-04-29",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Hackensack",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71880",
      "recalling_firm": "Elcam Medical, Inc.",
      "address_1": "2 University Plz Ste 620",
      "address_2": "N/A",
      "postal_code": "07601-6224",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Texas, New Mexico and Pennsylvania",
      "recall_number": "Z-2749-2015",
      "product_description": "Elcam Medical MANI 3G Plate BLS RAD B.BRAUN; Manifold for pressure monitoring and intravenous fluid administration.  Manufactured by: Elcam Medical ACAL, Israel; Distributed by: Elcam Medical Inc., USA. Sterile",
      "product_quantity": "248,100",
      "reason_for_recall": "Punctured blister packages were detected during the packaging process at the manufacturing site. Potential for device contamination.",
      "recall_initiation_date": "20150719",
      "center_classification_date": "20150910",
      "termination_date": "20170918",
      "report_date": "20150916",
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