Skip to main content

Smith¿s Medical ASD, Inc.

FDA adverse event reports naming Smith¿s Medical ASD, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SMITH¿S MEDICAL ASD, INC..

Total reports

1,247

Breakdown unavailable for this manufacturer. FDA filed these reports under a name containing characters the openFDA search API cannot match, so the death, injury and malfunction split, the yearly trend and the device categories can't be retrieved. The total above comes from openFDA's manufacturer index, which does return the name.

This is a limitation of the FDA's public API, not a gap in the underlying reports.

Monitor Smith¿s Medical ASD, Inc. automatically

DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.