{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "San Clemente",
      "address_1": "951 Calle Amanecer",
      "reason_for_recall": "ICU Medical Inc. has identified a potential risk of leaking with certain Tego Connector devices.",
      "address_2": "",
      "product_quantity": "476,600 units",
      "code_info": "3239841  3239848  3244021  3244022  3244023  3244558  3244560  3246196  3254636  3255850  3258004  3258326  3258327  3260656  3261516  3261517  3265975  3268523  3269593  3269594  3275467  3278966  3278967  3224799",
      "center_classification_date": "20170110",
      "distribution_pattern": "Worldwide Distribution-US: (Nationwide) and countries of: Saudi Arabia, Germany, Austria, Belgium, Estonia, Poland, Switzerland, Canada, Luxembourg, Netherlands, Bulgaria, Malaysia, Italy, Ireland, Great Britain, France, Brazil, Sweden, Slovenia, and Portugal.",
      "state": "CA",
      "product_description": "Tego Connector, Item No. D1000, NM1000    The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids to a patient through a cannula or needle placed in the vein or artery. The Tego¿ is a needle-free capping device which closes the end of the catheter. The Tego¿ will permit access to the catheter without the use of needles and therefore passively aid in the reduction of needle stick injuries.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ICU Medical, Inc.",
      "recall_number": "Z-0988-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75093",
      "termination_date": "20170707",
      "more_code_info": "",
      "recall_initiation_date": "20160824",
      "postal_code": "92673-6212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}