Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aliquot Delivery Kit (Syringe and Plunger) Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to Two isolated instances of holes in the outer...
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 Orthovita, Inc., dBA Stryker Orthobiologics. directly.
Affected Products
Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous procedures to facilitate placement of bone cement in weakened or diminished bone
Quantity: 9805
Why Was This Recalled?
Two isolated instances of holes in the outer header bag component of the double barrier sterile packaging configuration
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Orthovita, Inc., dBA Stryker Orthobiologics.
Orthovita, Inc., dBA Stryker Orthobiologics. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report