Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle 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 Bone Marrow Aspiration Needle, Model Numbers: 2090-0027 Needle (bullet-tip), 11 gauge x 4 inch 2090-0028 Needle (bullet-tip), 11 gauge x 6 inch 2090-0029 Needle (bullet-tip), 8 gauge x 6 inch 2090-0047 Needle (bullet-tip), 8 gauge x 8 inch 2090-0030 Needle (bullet-tip), Fenestrated, 8 gauge x 6 inch intended for use to aspirate bone marrow or autologous blood.
Quantity: 89770
Why Was This Recalled?
There is the potential for a breach in the inner or outer packaging pouches of all lots of the Imbibe Bone Marrow Aspiration 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