Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model Numbers: Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to There is the potential for a breach in...
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
Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model Numbers: 2110-0505 Beveled Needle, 11 gauge x 4 inch 2110-0524 Beveled Needle, 11 gauge x 6 inch 2110-0506 Diamond Needle, 11 gauge x 4 inch 2110-0529 Diamond Needle, 11 gauge x 6 inch Intended Use: Can be used in either direct (or open) and percutaneous (or deep) delivery of bone cement.
Quantity: 2155
Why Was This Recalled?
There is the potential for a breach in the inner or outer packaging pouches of all lots of the Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle.
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