{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "203889",
      "product_res_number": "Z-0357-2024",
      "event_date_initiated": "2023-09-29",
      "event_date_posted": "2023-11-21",
      "recall_status": "Open, Classified",
      "res_event_number": "93313",
      "product_code": "CHL",
      "k_numbers": [
        "K161818",
        "K992834"
      ],
      "product_description": "GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Part Numbers 00024307504, 00024330004, 00024345004",
      "code_info": "Part No. 00024307504:\nUDI-DI: 08426950087922,\nLot Numbers: 324230M, 323630G;\n\nPart No. 00024330004:\nUDI-DI: 08426950082507,\nLot Numbers: 325655C, 322355C, 323755H, 323855E, 326255D;\n\nPart No. 00024345004:\nUDI-DI: 08426950082538,\nLot Numbers: 325660C, 324160J, 323760H",
      "firm_fei_number": "1217183",
      "recalling_firm": "Instrumentation Laboratory",
      "address_1": "180 Hartwell Rd",
      "city": "Bedford",
      "state": "MA",
      "postal_code": "01730-2443",
      "additional_info_contact": "Technical Support Center\n800-678-0710",
      "reason_for_recall": "Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications for pO2. The positive bias may lead to false positive for medical decision levels at pO2 < 60 mmHg, which may result in failure to detect and/or adequately treat hypoxemia and lead to a delay in treatment. The quality control procedures for the Non-iQM GEM Premier 3000 may not detect the non-conformance.",
      "root_cause_description": "Under Investigation by firm",
      "action": "An URGENT MEDICAL DEVICE RECALL notification letter dated 9/29/23 was sent to customers.\n\nMandatory Customer Actions\nPlease take the following immediate actions:\n\" Check your inventory for the GEM Premier 3000 Non-iQM PAK (cartridge) lot numbers listed in Appendix A.\n\" Discontinue use and destroy any GEM Premier 3000 Non-iQM PAK (cartridge) lot numbers listed in Appendix A.\n\" Document the destruction on the Mandatory Tracking Response Record and return the completed and signed form to Werfen Regulatory at the fax number or e-mail address listed below.\n\" Contact Werfen Customer Service at 1-800-955-9525 to order replacement PAKs (cartridges).\n\" Share this information with your laboratory staff and follow your internal procedures.\n\" Forward this notification to all affected locations within your facility.\n\" Retain a copy of this notification for your records.\n\nMandatory Response Tracking Record\n\" Return the completed and signed Mandatory Response Tracking Form to:\n\" Fax No.: 1-781-861-4207\nOr\n\" E-mail: ra-usa.na@werfen.com\n\nContact Information for Questions\n\" For technical questions, contact the Technical Support Center at 1-800-678-0710.\n\" For replacement cartridges, contact Customer Service at 1-800-955-9525.",
      "product_quantity": "2448 total",
      "distribution_pattern": "US States: MA, MN, NY. India.",
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        "device_name": "Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.1120",
        "device_class": "2",
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