Medical Device Recalls: Ad-Tech Medical Instrument Corporation, Subdural Electrodes

You are subscribed to Medical Device Recalls for U.S. Food & Drug Administration (FDA). Information about the Ad-Tech Medical Instrument Corporation, Macro Micro Subdural Electrodes Class I Recall has recently been updated, and is now available. Manage your FDA Subscriptions: Update your preferences or unsubscribe Questions about this service? support@govdelivery.com Other inquiries? webmail@oc.fda.gov This email was sent to clotito+biotechdash@gmail.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420