Servo-I ventilator system CO2 analyzer. Part number 65 23 588.
FDA Device Recall #Z-1224-2015 — Class II — January 12, 2015
Recall Summary
| Recall Number | Z-1224-2015 |
| Classification | Class II — Moderate risk |
| Date Initiated | January 12, 2015 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Maquet Cardiovascular Us Sales, Llc |
| Location | Wayne, NJ |
| Product Type | Devices |
| Quantity | 486 units |
Product Description
Servo-I ventilator system CO2 analyzer. Part number 65 23 588.
Reason for Recall
A calibration problem was detected in a specific number of the Servo-I ventilator system CO2 analyzer models that may have been caused by the module's internal circuit board function.
Distribution Pattern
Worldwide distribution - USA nationwide, Austria, Australia, Belgium, Chile, Canada, Colombia, Ecuador, Egypt, Finland, France, Germany, Hungary, Iceland, India, Indonesia, Iraq, Italy, Japan, Libya, Netherlands, Norway, Panama, Peru, Portugal, Romania, Russia, Saudi Arabia, South Africa, Spain, Sweden, Thailand, Tunisia, Turkey, Ukraine, and United Kingdom.
Lot / Code Information
Serial Numbers: 9592 9604 9606 9608 9609 9610 9611 9612 9616 9617 9618 9619 9620 9621 9625 9626 9627 9636 9643 9645 9646 9647 9648 9649 9650 9651 9652 9653 9654 9655 9656 9657 9658 9659 9660 9661 9662 9664 9666 9667 9668 9669 9670 9671 9674 9676 9677 9678 9679 9680 9681 9682 9683 9684 9686 9687 9689 9690 9692 9697 9698 9702 9706 9708 9709 9712 9716 9718 9720 9721 9727 9732 9739 9747 9748 9752 9754 9755 9756 9757 9760 9763 9764 9765 9767 9770 9772 9774 9775 9777 9779 9782 9784 9785 9787 9788 9789 9793 9794 9795 9797 9799 9801 9802 9804 9805 9806 9808 9809 9810 9812 9813 9814 9815 9816 9817 9818 9819 9820 9821 9822 9823 9824 9825 9826 9827 9828 9829 9830 9831 9832 9833 9834 9836 9837 9838 9839 9840 9841 9860 9887 9891 9893 9894 9901 9902 9907 9908 9909 9916 9917 9922 9925 9934 9935 9937 9939 9941 9945 9946 9953 9954 9958 9959 9961 9963 9967 9991 10003 10004 10005 10006 10007 10008 10009 10010 10011 10012 10013 10018 10019 10020 10021 10022 10023 10024 10027 10029 10032 10060 10064 10070 10078 10079 10080 10082 10083 10084 10085 10086 10091 10092
Other Recalls from Maquet Cardiovascular Us Sales, Llc
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0632-2021 | Class II | HLS Set Advanced Model Name: BEQ-HLS 5050 USA; ... | Nov 20, 2020 |
| Z-0633-2021 | Class II | HLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS ... | Nov 20, 2020 |
| Z-0443-2021 | Class II | Blood Monitoring Unit (BMU 40), model no. 70104... | Sep 30, 2020 |
| Z-0133-2021 | Class II | Yuno II Mobile Operating Table - Product Usage:... | Sep 24, 2020 |
| Z-0132-2021 | Class II | Yuno Mobile Operating Table - Product Usage: In... | Sep 24, 2020 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.