{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "40858",
      "product_res_number": "Z-0157-06",
      "event_date_initiated": "2005-08-01",
      "event_date_posted": "2005-11-17",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-11-16",
      "res_event_number": "32810",
      "product_code": "KDP",
      "k_numbers": [
        "K853095"
      ],
      "product_description": "Boehringer Suction Regulator Model number 3714",
      "code_info": "Lot number 05F",
      "firm_fei_number": "2518417",
      "recalling_firm": "Boehringer Laboratories, Inc.",
      "address_1": "500 E Washington St",
      "city": "Norristown",
      "state": "PA",
      "postal_code": "19401-5149",
      "additional_info_contact": "John Karpowicz\n610-278-0900",
      "reason_for_recall": "Condition exists that prevents complete shutoff of the valve",
      "root_cause_description": "Other",
      "action": "The recalling firm telephoned their customers on 7/25/05 to inform them of the problem, request the return of the recalled product,  and inform them that replacement products were being shipped",
      "product_quantity": "1829 units",
      "distribution_pattern": "The products were shipped to hospitals AZ, AK, CA, FL, LA, MI, MO, NC, NJ, OR, PA, SC, UT, VA, and WA.",
      "openfda": {
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        "device_name": "Regulator, Vacuum",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6740",
        "device_class": "2"
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}