{
  "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": "Ronkonkoma",
      "address_1": "2 Fleetwood Ct",
      "reason_for_recall": "Microbial contamination of Non Sterile Product; contamination with Burkholderia cepacia (manufacturer)",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Antiseptic wipes shipped since July 02, 2009. Lots:  JT14509,  JT15209, JT20609, JT20909, JT23709, JT27809,  JT32809, JT00710,  JT15810,  JT18310,  JT18810,  JT23210,  JT25810,  JT27610,  JT31510,  JT35610,  JT35911,  JT04811,  JT05311,  JT11811,  JT15211,  JT15911,  JT18211,  JT18211,  JT21511-1,  JT26311,  JT30711,  JT22011-1,  JT01012,  JT04112,  JT06512, JT07512, JT07710,  JT14509, JT15209,  JT21409,  JT20609, JT33009,  JT00710,  JT18810, JT23210,  JT35911,  JT05311,  JT11811,  JT26311,  JT01012,  JT14509,  JT15209,  JT20609,  JT15209,  JT23709,  JT27809,  JT00710,  JT00710,  JT18310,  JT18810,  JT23210,  JT23210,  JT27610,  JT31510, JT05809,  JT14509,  JT15209,  JT21209,  JT27809,  JT12510,  JT15810,  JT18310,  JT11811,  JT13211,  JT15911,  JT35911,  JT01012,  JT30711",
      "center_classification_date": "20120917",
      "distribution_pattern": "Nationwide",
      "state": "NY",
      "product_description": "ZEE Antiseptic Wipes, First Aid Antiseptic, Benzalkonium chloride 0.133% (effective concentration), over the counter; supplied in 10 (item 2633), 50 (items 0204 and 02040 [sold in Canada only]) and 100 (item 0271) wipes per box distributed by ZEE MEDICAL, INC., Irvine, CA",
      "report_date": "20120926",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Dukal Corp.",
      "recall_number": "D-1675-2012",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "62320",
      "termination_date": "20130621",
      "more_code_info": "",
      "recall_initiation_date": "20120614",
      "postal_code": "11779-6907",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}