{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Fajardo",
      "address_1": "Calle Igualdad Final #7",
      "reason_for_recall": "Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.",
      "address_2": "",
      "product_quantity": "4 lots/972 units (multiple units per lot)",
      "code_info": "Product code 900-2473 ,4 lots  112020354  112051960  112072724  113057469",
      "center_classification_date": "20140829",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) in the state of  Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.",
      "state": "PR",
      "product_description": "ARTHROSCOPY PACK I (1)   CUSTOMED    CONTENTS:\t  (1) \tTOWELS ABSORBENT 15\" X 20\"    (1) \tGOWN XL SMS IMPERVIOUS REINFORCED (1) \tMAYO STAND COVER  REINFORCED  (1) \tU - DRAPE 60\" X 70\" WITAPE SPLIT 6 X 21    (1) \tSHEET SPLIT W/ADHESIVE 108\" X 77\" STD SMS (1) \tSTOCKINETTE IMPERVIOUS  12\" X 48\"  (4) \tSTRIPS TAPE 24\" X 4\"    (1) \tSUTURE BAG FLORAL    (1) \t SHEET ARTHROSCOPY  T STD SMS W/ POUCH (1) \tTABLE COVER  REINFORCED 44\" X 78\"  (1) \tGOWN SURG. REINFORCED XLGE TOWEL I WRAP    Product Usage:  EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.",
      "report_date": "20140910",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Customed, Inc",
      "recall_number": "Z-2462-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68536",
      "termination_date": "20170814",
      "more_code_info": "",
      "recall_initiation_date": "20140520",
      "postal_code": "00738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}