{
  "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": [
    {
      "status": "Terminated",
      "city": "Toano",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76745",
      "recalling_firm": "Avid Medical, Inc.",
      "address_1": "9000 Westmont Dr",
      "address_2": "N/A",
      "postal_code": "23168-9351",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "All products are distributed through distribution centers confined to the US. All end-users for these products are also solely located in the US.",
      "recall_number": "Z-1865-2017",
      "product_description": "Vacutainer Tubes  Vacutainer tubes are intended for clinical laboratory hematology studies including but not limited to lead level testing, FEP level testing, and CBC testing.",
      "product_quantity": "25308",
      "reason_for_recall": "Avid Medical Inc has received a complaint was received from an end-user indicating the vacutainer component 519700 (BD: 367863) expiring 12/16 was discovered inside of a kit labelled with an expiration date after 12/16. Upon receipt of complaint, AVID Medical promptly initiated an internal investigation and root cause analysis. Investigation found mixed component lots were contained in product 519700 component case.   This occurrence resulted in the incorrect lot number and expiration being attributed to all work orders produced using the affected component. This issue was immediately contained and corrected. A full inventory analysis was conducted reviewing all vacutainer component inventories. The issue was found to affect a total of five vacutainer components.",
      "recall_initiation_date": "20170315",
      "center_classification_date": "20170419",
      "termination_date": "20170907",
      "report_date": "20170426",
      "code_info": "Part Number/Product Number    ILEY029-01  ULKY005-14  LOUS015-03  DNAZ017-01    ILEY029-02  SERA003-07  TENN016-05  DONS008-05  EVER007  SERA005-07  LANC029-06  STLM007-10  CCHM024-03    Part Number/Product Number    LANC015-27  CCHM027-04  STLM003-11  ABIN137-01  ABIN110-01  LANC015-28  MONT045-03  ILEY003-53  NAFB015-07  ILEY014-21  ILEY034-04  ILEY034-05    Part Number/Product Number    AV10654-10  ILEY014-22  EVER010  EVER001  SOHS016-03  SSHH118-03  SSHH117-06  SOHS017-03  HCMH009-05  WIME023-08  TUFT040-05    Part Number/Product Number    TUFT039-08  HCMH009-06  GIFT022-01  TUFT040-06  PCHM004-07  HLDH008-04  WHWC005-17  PCHM008-04  LANC015-25  PCHM011-03"
    }
  ]
}