{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "158667",
      "product_res_number": "Z-0198-2018",
      "event_date_initiated": "2017-06-01",
      "event_date_created": "2017-12-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-05-09",
      "res_event_number": "78102",
      "product_code": "JQX",
      "product_description": "BD PhoenixTM AP, Catalog Number 448010\nThe BD Phoenix\" AP instrument is designed for use with the BD Phoenix\" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix\" system, which performs identification and susceptibility testing",
      "code_info": "Serial Numbers: AP0447, AP0448, AP0449, AP0450, AP0451, AP0458 & AP0463.",
      "firm_fei_number": "1119779",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Cir",
      "city": "Sparks",
      "state": "MD",
      "postal_code": "21152-9212",
      "additional_info_contact": "Gail Griffiths\n410-316-4258",
      "reason_for_recall": "Potential unexpected movement of robot arm",
      "root_cause_description": "Process control",
      "action": "BD Diagnostic Systems telephoned all customers on June 1, 2017 and sent an Urgent Product Recall letter dated May 31, 2017, and Response Forms to their customers via email.  BD recently confirmed a manufacturing issue with the motor that drives movement of the robot arm.  The issue may result in the inability of this motor to withstand the lateral forces encountered during normal operations.   Should this occur, the instrument will indicate an E20 error-Pipettor step loss during operation and stop functioning.  While there is no loss of patient sample, the samples would need to be manually processed until the instrument can be repaired.  To limit any disruption in the workload, BD Service will contact customers to schedule the instrument replacement.  \nCustomers are advised to complete and return the response form via email to BDRC2@aol.com.  Customers may continue to use the instrument until replacement is performed.  Customers with questions may contact BD (Customer/Technical) Support at 1-800-638-8663.\nFor questions regarding this recall call 410-316-4258.",
      "product_quantity": "7 units",
      "distribution_pattern": "Worldwide Distribution - US including CA, NC & TN\nInternationally: Canada",
      "openfda": {
        "k_number": [
          "K885263",
          "K962294",
          "K801362",
          "K771446",
          "K851253",
          "K851234",
          "K781554",
          "K772361",
          "K781644",
          "K780251",
          "K792045",
          "K801089",
          "K790103",
          "K922273"
        ],
        "registration_number": [
          "2050012",
          "1111096",
          "3009238284",
          "3008517993",
          "3008862790",
          "3038188172",
          "1530126",
          "1119779",
          "3027977508",
          "3006198300",
          "3006786907",
          "1924669",
          "8021914"
        ],
        "fei_number": [
          "2050012",
          "1111096",
          "3009238284",
          "3008517993",
          "3008862790",
          "3038188172",
          "1119779",
          "3027977508",
          "1000515493",
          "3006198300",
          "3002806332",
          "3006786907",
          "1924669"
        ],
        "device_name": "Nephelometer, For Clinical Use",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.2700",
        "device_class": "1"
      }
    }
  ]
}