Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by Stryker Spine Due to Stryker has received reports from customers indicating post-operative...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Spine directly.
Affected Products
Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the occiput.
Quantity: 1536 units (US) 880 (Foreign)
Why Was This Recalled?
Stryker has received reports from customers indicating post-operative fracture of the pin that connects the tulip head to the plate body.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Spine
Stryker Spine has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report