{
  "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": "2026-08-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lawrence",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99433",
      "recalling_firm": "OBP Medical Corporation",
      "address_1": "360 Merrimack St Ste 9",
      "address_2": "",
      "postal_code": "01843-1764",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, \tIA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, \tOR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV and the countries of HKG, CAN, NOR, UAE.",
      "recall_number": "Z-2933-2026",
      "product_description": "OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small  REF: C020130-1",
      "product_quantity": "8,224 boxes (148,032 units)",
      "reason_for_recall": "There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.",
      "recall_initiation_date": "20260713",
      "center_classification_date": "20260810",
      "report_date": "20260819",
      "code_info": "UDI: (01)20888937027451/ Lots: 24J1202Z, 25D2302Z, 25A0202Z, 25E1502Z, 25B2802Z, 25L0802Z",
      "more_code_info": ""
    }
  ]
}