{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "50072",
      "product_res_number": "Z-0674-2007",
      "event_date_initiated": "2007-01-26",
      "event_date_posted": "2007-04-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-06-15",
      "res_event_number": "37188",
      "product_code": "BTI",
      "k_numbers": [
        "K982789"
      ],
      "product_description": "Medical Air Compressor  \nModel #8413419",
      "code_info": "Model number 8413419. Catalog number 8413419.  Serial Numbers ARXC-001; ARXC-0002; ARXC-0009; ARXC-0011; ARXC-0012; ARXC-0013; ARXC-0014; ARXC-0015; ARXC-0016; ARXC-0017; ARXC-0019; ARXC-0020; ARXD-0034; ARXD-0035; ARXD-0036; ARXD-0037; ARXD-0038; ARXD-0039; ARXD-0040; ARXE-0081; ARXE-0082; ARXE-0083; ARXE-0084; ARXE-0085; ARXE-0086; ARXE-0087; ARXE-0088; ARXE-0089; ARXE-0090; ARXE-0091; ARXE-0092; ARXE-0093; ARXE-0094; ARXE-0095; ARXE-0096; ARXE-0097; ARXE-0098; ARXE-0099; ARXE0100; ARXE-0101; ARXE-0102; ARXE-0103; ARXE-0104; ARXE-0106; ARXE-0107; ARXE-0108; ARXE-0109; ARXE-0110; ARXE-0111; ARXE-0112; ARXE-0113; ARXE-0114; ARXE-0115; ARXE-0116; ARXE-0117; ARXE-0118; ARXE-0119; ARXE-0120; ARXE-0121; ARXE-0122; ARXE-0123; ARXE-0124; ARXE-0125; ARXE-0126; ARXE-0127; ARXE-0128; and ARXE-0129.",
      "firm_fei_number": "2517967",
      "recalling_firm": "Draeger Medical, Inc.",
      "address_1": "3135 Quarry Rd",
      "city": "Telford",
      "state": "PA",
      "postal_code": "18969-1042",
      "additional_info_contact": "Mike Kelhart\n215-660-2349",
      "reason_for_recall": "Compressors not providing sufficient supply pressure to connected medical ventilator",
      "root_cause_description": "Other",
      "action": "The recalling firm issued a Medical Device Recall Letter dated 1/22/07 to their customers via Certified Mail.  An authorized service representative will inspect each potentially affected device.  If a device is found to have an affected dryer assembly, it will be repaired free of charge.",
      "product_quantity": "67 units",
      "distribution_pattern": "Nationwide.",
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        "device_name": "Compressor, Air, Portable",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.6250",
        "device_class": "2",
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