Medtronic Forced to Recall their Endotracheal Tubes After Complaints of Airway Obstruction (Health & Beauty - Health Services)
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Medtronic Forced to Recall their Endotracheal Tubes After Complaints of Airway Obstruction | |
In an incident that the FDA, Food and Drug Administration termed a Class 1 event, the most severe kind of recall, Medtronics, a medical device firm, had to recall endotracheal tubes from across the globe. The American medical firm termed the incident “rare instances of serious adverse events related to certain EMG endotracheal tubes.” Medtronics is a worldwide leader in medical services, technology For more details please visit our website - https://www.medhealthreview.com/2022/09/05/medtronic-forced-to-recall-their-endotracheal-tubes-after-complaints-of-airway-obstruction/  | |
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| Target State: New York Target City : New York City Last Update : Jul 14, 2025 2:13 AM Number of Views: 18 | Item Owner : medhealthreview Contact Email: Contact Phone: +1 702-213-6364 |
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2025-07-16 (0.444 sec)