{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72237",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "N/A",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationally",
      "recall_number": "Z-0150-2016",
      "product_description": "Perifix Continous Epidural Anesthesia Pain Control Trays; Injection of anesthetics to provide regional anesthesia for pain management.",
      "product_quantity": "433",
      "reason_for_recall": "Potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilization performed by the supplier.",
      "recall_initiation_date": "20150827",
      "center_classification_date": "20151021",
      "termination_date": "20160629",
      "report_date": "20151028",
      "code_info": "Product Catalog Number:  332215  332262  530024  530132  551714  551879  555184  555259  Lot Number  0061417406  0061421878  0061416371  0061420212  0061413247  0061416388  0061416389  0061414413"
    }
  ]
}