{
  "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": [
    {
      "country": "United States",
      "city": "Rifton",
      "address_1": "2032 Route 213",
      "reason_for_recall": "A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.",
      "address_2": "",
      "product_quantity": "167",
      "code_info": "ID Codes:  K66020170425AA  K66020170612AA  K66020170621AA  K66020170622AA  K66020170626AA  K66020170626AB  K66020170626AC  K66020170627AC  K66020170627AD  K66020170628AA  K66020170629AA  K66020170703AA  K66020170705AA  K66020170711AA  K66020170712AA  K66020170712AC  K66020170713AB  K66020170713AC  K66020170716AA  K66020170717AA  K66020170717AB  K66020170804AA  K66020170805AA  K66020170807AA  K66020170810AA  K66020170810AB  K66020170811AA  K66020170811AC  K66020170815AA  K66020170817AB  K66020170817AC  K66020170818AC  K66020170831AA  K66020170831AB  K66020170906AA  K66020170906AB  K66020170911AA  K66020170911AB  K66020170911AC  K66020170913AA  K66020170914AA  K66020170915AA  K66020170921AA  K66020170923AA  K66020170926AA  K66020170927AA  K66020170928AA  K66020171004AA  K66020171006AA  K66020171006AB  K66020171007AA  K66020171010AA  K66020171010AB  K66020171019AA  K66020171020AA  K66020171024AA  K66020171026AA  K66020171026AB  K66020171026AC  K66020171028AA  K66020171030AA  K66020171101AA  K66020171101AB  K66020171103AC  K66020171107AA  K66020171107AB  K66020171116AA  K66020171121AA  K66020171127AA  K66020171127AB  K66020171128AA  K66020171128AB  K66020171129AA  K66020171206AA  K66020171207AA  K66020171209AA  K66020171214AA  K66020171215AA  K66020171216AA  K66020171219AA  K66020171227AA  K66020171227AC  K66020180102AA  K66020180104AA  K66020180109AA  K66020180109AB  K66020180113AA  K66020180113AB  K66020180117AA  K66020180118AA  K66020180120AA  K66020180124AA  K66020180126AA  K66020180130AA  K66020180130AB  K66020180131AA  K66020180131AC  K66020180203AA  K66020180206AA  K66020180206AB  K66020180208AB  K66020180209AA  K66020180213AA  K66020180216AA  K66020180220AA  K66020180220AB  K66020180220AC  K66020180221AA  K66020180226AA  K66020180227AA  K66020180227AB  K66020180306AA  K66020180309AA  K66020180312AA  K66020180322AA  K66020180326AB  K66020180403AA  K66020180405AA",
      "center_classification_date": "20191022",
      "distribution_pattern": "The products were distributed US nationwide.    The products were distributed to the following foreign countries:  Foreign Countries: Worldwide, including Canada, United  Kingdom, Germany, Japan, Singapore, South Korea,  United Arab Emirates, Taiwan, Denmark, Italy, Hong  Kong, Ireland, Australia, New Zealand, Israel, Colombia,  Russia",
      "state": "NY",
      "product_description": "Rifton E-Pacer, SKU K660, powered lift device",
      "report_date": "20191030",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Community Products, LLC",
      "recall_number": "Z-0166-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "82607",
      "termination_date": "20200615",
      "more_code_info": "",
      "recall_initiation_date": "20190321",
      "postal_code": "12471",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}