Medical Device Safety and Recalls: Stryker Spine - OASYS Midline Occiput Plate

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Medical Device Safety and Recalls: Stryker Spine - OASYS Midline Occiput Plate

You are subscribed to receive updates about Medical Device Safety and Recalls for the U.S. Food & Drug Administration (FDA). Information about the Stryker Spine - OASYS Midline Occiput Plate Class I Recall has recently been posted.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@xxxxxxxxxxxxxxx
• Other inquiries? webmail@xxxxxxxxxx

---

This email was sent to list-fda@xxxxxxxxxxx using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420