{
  "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": "West Chester",
      "address_1": "1301 Goshen Pkwy",
      "reason_for_recall": "DePuy Synthes is voluntarily initiating this recall due to affected devices that were distributed, etched and or labeled with MR Safety information not meeting the current ASTM standard.",
      "address_2": "",
      "product_quantity": "19 units",
      "code_info": "Part # 313.250, 1.1mm Drill Bit, Mini QC with 4mm Stop/44.5mm, lot # 4326989, mfg. 9/28/2001",
      "center_classification_date": "20160712",
      "distribution_pattern": "US Nationwide Distribution in the states of: AR,CA,CO,CT,DC,ID,IL,KY,LA,MA,MD,MN,MO,MS,MT,NY,PA and TX.",
      "state": "PA",
      "product_description": "Part # 313.250, 1.1mm Drill Bit, Mini QC with 4mm Stop/44.5mm, lot # 4326989, mfg. 9/28/2001    Product Usage:  The DePuy Synthes MR Safe Instruments and MR conditional Instruments are used to assist with the insertion or removal of an implant.",
      "report_date": "20160720",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes (USA) Products LLC",
      "recall_number": "Z-2199-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74416",
      "termination_date": "20170202",
      "more_code_info": "",
      "recall_initiation_date": "20160531",
      "postal_code": "19380-5986",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}