{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Buffalo Grove",
      "address_1": "485 E Half Day Rd Ste 320",
      "reason_for_recall": "Devices were not sterilized",
      "address_2": "",
      "product_quantity": "1763",
      "code_info": "SKU 17161; Lot 5A22",
      "center_classification_date": "20150326",
      "distribution_pattern": "Nationwide Distribution including CA, FL, GA, IA, IL, IN, LA, MA, MD, MO, MS, NC, NJ, NY, OK, PA, RI, SC, TN, TX, UT, VA, and WA.",
      "state": "IL",
      "product_description": "Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75\") within a secondary corrugated shipper (16 x 11.02 x 5.12\" inner dimensions).  The device is indicated for assisted expression of milk using manual suction.",
      "report_date": "20150401",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ameda, Inc.",
      "recall_number": "Z-1326-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70599",
      "termination_date": "20170721",
      "more_code_info": "",
      "recall_initiation_date": "20150212",
      "postal_code": "60089-8806",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}