{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Somerville",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83715",
      "recalling_firm": "Ethicon, Inc.",
      "address_1": "Us Highway 22 West",
      "address_2": "N/A",
      "postal_code": "08876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "States:  IN  MD  AR  IL  GA  TN  NJ  PA  NC  CA  OK  CO  KS  UT  KY  WA  OH  OR    OUS:  Australia  Hong King  India  Japan  Korea  Singapore  Thailand  United States",
      "recall_number": "Z-0047-2020",
      "product_description": "STRATAFIX Spiral PDS Plus Violet 18  (45cm) CT-1 Needle  Product code: SXPP1B430  suture",
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      "reason_for_recall": "The product does not meet certain internal strength testing specifications.",
      "recall_initiation_date": "20190813",
      "center_classification_date": "20191004",
      "termination_date": "20210211",
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}