The U.S. Food and Drug Administration announced March 24 that it is alerting health care professionals, patients and caregivers of EpiPen autoinjector errors related to device malfunctions and user administration.
Recent Posts
- Small business loan provisions in CARES Act analyzed
- ADA joins other health care organizations in appeal for more PPE, other supplies
- University of Washington School of Dentistry appoints Dr. Gary Chiodo as dean
- University of Minnesota dental school appoints Dr. Keith A. Mays as interim dean
- House passes CARES Act
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