{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "2441 Michelle Dr",
      "reason_for_recall": "The firm initiated this recall of certain Toshiba Diagnostic Ultrasound Systems because it has been found that under certain conditions, the temperature of the transducer head may increase in 2D+PW mode or 2D+CDI (POWER, ADF) +PW mode. When the system is used under both conditions listed below, the temperature of the transducer head connected to the system may increase in temperature and possibly",
      "address_2": "P.O. Box 2068",
      "product_quantity": "430 (1352 total)",
      "code_info": "Lot Numbers not utilized.  Serial Numbers:  99D0833447  99E0873714  99G0995029  99D0823343  99F0924404  99G09Y5216  99E0863552  99E0863553  99G0964771  99C0792920  99F0893870  99B06Z2073  99C07X2964  99C0792918  99B06Z2063  99C0792919  99G0964712  99G0964713  99G0974899  99F0944563  99D0823349  99G0995131  99G0995132  99G0995133  99G0995134  99G09Y5224  99C0792914  99D0813229  99D0813230  99D0813231  99E0873711  99E0873716  99E0873717  99B06Z2072  99B0752508  99B0752509  99B0752510  99B0752511  99C0792915  99C0792937  99F0893967  99F08Y4079  99F08Y4085  99F08Y4086  99F0924389  99F0924395  99F0924405  99B06Z2107  99G1045683  99C07Y3068  99C07Y3069  99B0782760  99C07Y3047  99B0722268  99B0722269  99B0722270  99B0722271  99B0722272  99B0732349  99B0732350  99B0732351  99B0732352  99B0732353  99B0732354  99E0863691  99E0863692  99G0995139  99B0722208  99B0722250  99F0934520  99C0782863  99B06Z2061  99G0995071  99G09Y5260  99G09Y5261  99D0813225  99D0813226  99E0863586  99E0863587  99C0782860  99G0964777  99B0752531  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      "center_classification_date": "20131030",
      "distribution_pattern": "Nationwide Distribution including and US Territory Puerto Rico",
      "state": "CA",
      "product_description": "Aplio XG Diagnostic Ultrasound System SSA-790A    Used for routine diagnostic imaging",
      "report_date": "20131106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-0122-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66059",
      "termination_date": "20160628",
      "recall_initiation_date": "20130805",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}