{
  "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": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89163",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and Canada.",
      "recall_number": "Z-0506-2022",
      "product_description": "Infant Heel Warmers w/strap, Reference # 989805603201 1223",
      "product_quantity": "5,164,600 units",
      "reason_for_recall": "After the device was cleared by the FDA, Philips made changes to the labeling that do not fall within the  existing FDA clearance. These devices with the modified labeling cannot be distributed or sold without  new 510(k) clearance.",
      "recall_initiation_date": "20211129",
      "center_classification_date": "20220119",
      "report_date": "20220126",
      "code_info": "All units are impacted"
    }
  ]
}