{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "29961",
      "product_res_number": "Z-0288-04",
      "event_date_initiated": "2003-10-17",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-10-11",
      "res_event_number": "27490",
      "product_code": "FMZ",
      "k_numbers": [
        "K020543"
      ],
      "product_description": "Radiant Heater Door Vent for Ohmeda Medical''s Giraffe (tm) OmniBed neonate bed.",
      "code_info": "HDGDyyyyy HDGEyyyyy HDGFyyyyy HDGGyyyyy where ''yyyyy'' represents any number less than 60000",
      "firm_fei_number": "1121732",
      "recalling_firm": "Ohmeda Medical, A Div of Datex-Ohmeda , Inc",
      "address_1": "8880 Gorman Rd",
      "city": "Laurel",
      "state": "MD",
      "postal_code": "20723-5800",
      "additional_info_contact": "Alberto Profumo\n410-888-5204",
      "reason_for_recall": "Heater vent door on neonatal incubator may malfunction.",
      "root_cause_description": "Other",
      "action": "The recalling firm notified domestic consignees by certified letter and international distributors by e-mail dated 10/17/2003. The recall notice was incorporated into a firm''s follow-up letter concerning an on-going product correction of the elevating base on the same neonatal beds. The letter advises of the malfunctioning heater door vent and states that the firm will replace all existing vent doors with doors made of higher temperature rated material. Firm will provide retrofit kits for consignee or service representative installation.",
      "product_quantity": "1404 beds",
      "distribution_pattern": "Products were sold to 365 direct accounts around the US and 58 international distributors.",
      "openfda": {
        "k_number": [
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        "device_name": "Incubator, Neonatal",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5400",
        "device_class": "2",
        "registration_number": [
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}