{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Swedesboro",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86607",
      "recalling_firm": "Thomas Scientific",
      "address_1": "1654 High Hill Rd",
      "address_2": "N/A",
      "postal_code": "08085-1780",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KA, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.",
      "recall_number": "Z-0449-2021",
      "product_description": "Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.",
      "product_quantity": "115,800 cs (100 vials/cs)",
      "reason_for_recall": "The firm is replacing all tubes that were manufactured and distributed prior to Enforcement Discretion Approval.",
      "recall_initiation_date": "20200714",
      "center_classification_date": "20201113",
      "report_date": "20201125",
      "code_info": "Lots   060620MB1   061420MB2   062120MB1   062220MB2   060620MB2   052220MB1   051820D01   060120D01   061520MA1   062220D02   061720MB1   052720D02   061920E01   052120E01"
    }
  ]
}