{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "42291",
      "product_res_number": "Z-0102-06",
      "event_date_initiated": "2005-09-13",
      "event_date_posted": "2005-10-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-03-03",
      "res_event_number": "33691",
      "product_code": "JOZ",
      "k_numbers": [
        "K992531"
      ],
      "product_description": "Accumetrics part number 29001 VerifyNow Instrument, printe power supply",
      "code_info": "lot number G-13850",
      "firm_fei_number": "3001376288",
      "recalling_firm": "Accumetrics Inc",
      "address_1": "3985 B Sorrento Valley Blvd",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121",
      "additional_info_contact": "Roberta G. Hoffman\n888-919-9333 Ext. 218",
      "reason_for_recall": "In 2001, separate reports of mild shock, sparking and smoke from Accumetrics PN 29001 power supply.",
      "root_cause_description": "Other",
      "action": "Letters and replacement power supplies were sent to consignees by Fedex, 2-day with proof of delivery.  End-user customers were instructed to return the affected power supply to Accumetrics, using the provided pre-paid shipping carton.  \n \nConsignees who do not return the power supply within two weeks of the notification will be contacted by phone to assess compliance with the recall and to determine the status of the product at the site.",
      "product_quantity": "11",
      "distribution_pattern": "CA, FL, IL, LA, NH, NV, NY, OK, WA",
      "openfda": {
        "k_number": [
          "K140893",
          "K791577",
          "K002885",
          "K012723",
          "K962426",
          "K191364",
          "K954997",
          "K041502",
          "K060489",
          "K851669",
          "K032951",
          "K940792",
          "K012701",
          "K781807",
          "K800146",
          "K970505",
          "K770395",
          "K161329",
          "K011337",
          "K042423",
          "K862302",
          "K103555",
          "K050265",
          "K800432",
          "K990398",
          "K163274",
          "K013596",
          "K141427",
          "K051231",
          "K781693",
          "K760893",
          "K790769",
          "K780285",
          "K181777",
          "K992531",
          "K122162",
          "K023761",
          "K780047"
        ],
        "registration_number": [
          "3003601075",
          "8020030",
          "3005269352",
          "3003455467",
          "1219343",
          "3016571810",
          "2518152",
          "1618982",
          "3002807408",
          "3019849102",
          "1217183",
          "3016579901",
          "9610806",
          "3002721930",
          "1000487132",
          "3005739529",
          "3017875469"
        ],
        "fei_number": [
          "3003601075",
          "3005269352",
          "3003455467",
          "3001644026",
          "1219343",
          "2250033",
          "3016571810",
          "2518152",
          "1618982",
          "3002807408",
          "3019849102",
          "1217183",
          "3006461677",
          "3016579901",
          "1000487132",
          "3005739529",
          "3017875469"
        ],
        "device_name": "System, Automated Platelet Aggregation",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.5700",
        "device_class": "2"
      }
    }
  ]
}