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All product recalls associated with Draeger Medical Systems, Inc..
Total Recalls
6
Past Year
1
Class I (Serious)
0
Most Recent
Jan 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Edifier speakers (shipped in or after April 2023) may not annunciate when configured in analog mode which can lead to delayed treatment to the patient.
Device is not in full compliance to Type CF requirements of IEC 60601-1 and IEC 60601-2-34 standards. Therefore, there is a potential risk of electric shock. Health consequences may include electrical shock, burns, and cardiac arrhythmia.
The Resuscitaire Infant Radiant Warmer with the optional scale could display inaccurate weight values.