{
  "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": "2026-08-20",
    "results": {
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  "results": [
    {
      "cfres_id": "32145",
      "product_res_number": "Z-0766-04",
      "event_date_initiated": "2004-02-23",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-01-04",
      "res_event_number": "28570",
      "product_code": "KYB",
      "product_description": "MicroSTAAR Injector w/ Foam Tip Plunger, Model MSI-PF",
      "code_info": "Lot 11853090.   Sterility Date : 11/18/2003 Expiration Date: 10/31/2006",
      "firm_fei_number": "2023826",
      "recalling_firm": "Staar Surgical Co Inc",
      "address_1": "1911 Walker Ave",
      "city": "Monrovia",
      "state": "CA",
      "postal_code": "91016-4846",
      "additional_info_contact": "Janice L. Filippelli\n626-303-7902 Ext. 2345",
      "reason_for_recall": "Injector mold design/manufacture and wear caused material flash to develop preventing assembly of the device prior to use.",
      "root_cause_description": "Other",
      "action": "Firm will be sending thier representatives to customers to inspect inventory and arrange return of product.",
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      "distribution_pattern": "Nationwide.",
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