{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Moorpark",
      "address_1": "11959 Discovery Ct",
      "reason_for_recall": "Complaints were received on the product, such as the re-breather bag would not fill/inflate or the oxygen line pops off after the oxygen is turned on due to a clogged port.",
      "address_2": "",
      "product_quantity": "5,610 units",
      "code_info": "Model 1001-MM - Lot numbers 021418-021421, 032218-032221, 032618-032621, and 032818-032821;    Model KE1001-MM, an internal number used by one of the distributors (same as 1001-MM) - Lot numbers 021418-021421 and 032818-032821;    Model 301-0318LT - Lot numbers 022218-022221, 032218-032221, 032618-032621; and    Model 1001-MF - Lot number 032818-032821.",
      "center_classification_date": "20191031",
      "distribution_pattern": "Distribution was made to CA, FL, MO, OH, and PA.",
      "state": "CA",
      "product_description": "POM Procedural Oxygen Masks, Endoscopic, Conscious Sedation, Bronchoscopy Mask, as follows:  (1) POM Medical, LLC, REF 1001-MM, High/Med Concentrations, Distributed by POM Medical, LLC, Moorpark, CA; (2) curaplex, REF 301-0318LT, Medium Concentration, Distributed by Sarnova HC, LLC's family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency Medical Products, Inc. & Tri-anim Health Services, Inc., Dublin, OH; and (3) POM Medical, LLC REF 1001-MF, High/Med Concentrations, Distributed by POM Medical, LLC, Moorpark, CA.  All are packaged 1 mask/plastic pouch, 30 masks/case.",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "POM Medical LLC",
      "recall_number": "Z-0262-2020",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "83540",
      "termination_date": "20210104",
      "more_code_info": "",
      "recall_initiation_date": "20180711",
      "postal_code": "93021-7120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}