Medical Device Recalls: Class I Recall of Synthes USA, Ti Synex II Vertebral Body Replacement (VBR)
You are subscribed to Medical Device Recalls for U.S. Food & Drug Administration (FDA). Information about the Synthes USA, Ti Synex II Vertebral Body Replacement (VBR) 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
GovDelivery, Inc. sending on behalf of U.S. Food & Drug Administration (FDA) · 5600 Fishers Lane · Rockville MD 20857 · 800-439-1420