- FDA Updates on Fungal Meningitis Outbreak
- FDA Questions and Answers on Fungal Meningitis Outbreak
- CDC Clinician Guidance on Fungal Meningitis Outbreak
- CDC Multistate Fungal Meningitis Outbreak Investigation
- NECC Press Release
Clinicians are also requested to report any suspected adverse events following use of these products to both FDA's MedWatch program at 1-800-332-1088 or www.fda.gov/medwatch and to the DPH Infectious Diseases Section at 860-509-7995.
Health care professionals may dial FDA’s Drug Information Line at 855-543-DRUG (3784) and press * to get the most recent information regarding the meningitis recall and speak directly to a pharmacist.
Guidance for Patients
Patients who are concerned that they may have received NECC products should contact their healthcare provider.