{
  "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": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83962",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide.",
      "recall_number": "Z-0302-2020",
      "product_description": "Various Custom Devices, Item Nos. 32855090246  32855090252  32855090256  32855090265  32855090266  32855090270  32855090287  32855090290  32855090291  32855090297  32855090302  32855090317  32855090318  32855090319  32855090327  32855090329  32855090334  32855090336  32855090339  32855090348  32855090351  32855090352  32855090353  32855090354  32855090368  32855090369  32855090375  32855090376  32855090395  32855090396  32855090402  32855090409  32855090414  32855090434  32855090437  32855090439  32855090448  32855090450  32855090465  32855090484  32855090496  32855090497  32855090498  32855090501  32855090507  32855090512  32855090519  32855090520  32855090531  32855090543  32855090576  32855090585  32855090586  32855090593  32855090598  32855090599  32855090609  32855090615  32855090622  32855090628  32855090636  32855090637  32855090638  32855090640  32855090658  32855090659  32855090661  32855090715  32855090734  32855510763  32855510796  32855510797  32855510799  32855510800  32855510801  32855510805  32855510808  32855510822  32855510843  32855510844  32855140373  32855411710  32855430479  32855430480  32855430496  32855430498  32855430519  32855430529  32855430533  32855430535  32855430542  32855430544  32855430582  32855430588  32855450430  32855450439  32855450471  32855450483  32855450525  32855470651  32855470715  32855470793  32855470795  32855470796  32855470866  32855470920  32855470921  32855470923  32855480803  32855480808  32855480823  32855480824  32855480828  32855480829  32855480945  32855480963  32855480990  32855481016  32855910440  32855910454  32855910455  32855910456  32855910475  32855910485  32873400307",
      "product_quantity": "5,459,583 total devices",
      "reason_for_recall": "Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).",
      "recall_initiation_date": "20191010",
      "center_classification_date": "20191107",
      "termination_date": "20200519",
      "report_date": "20191113",
      "code_info": "All product manufactured prior to January 2014."
    }
  ]
}