{
  "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": "Buffalo Grove",
      "address_1": "1110 W Lake Cook Rd",
      "reason_for_recall": "Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients along with the preservative, on the exterior of the bottles.",
      "address_2": "Ste 301",
      "product_quantity": "78 bottles",
      "code_info": "Lot #:NW3071. Exp. 06/15.",
      "center_classification_date": "20140204",
      "distribution_pattern": "Nationwide and Puerto Rico.",
      "state": "IL",
      "product_description": "Timolol Maleate Sterile Ophthalmic Solution, USP 0.25%, 10mL, (NDC 16571-140-10).     The products are packaged in Low Density Polyethylene (LDPE) Blow Fill Seal containers equipped with a dropper tip.  The filled bottles are individually packaged into fiberboard cartons.",
      "report_date": "20140212",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "PACK Pharmaceuticals, LLC",
      "recall_number": "D-1071-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "66595",
      "termination_date": "20140411",
      "more_code_info": "",
      "recall_initiation_date": "20130909",
      "postal_code": "60089-1944",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}