Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
3910-090-800 ASSY Recalled by Stryker Corporation Due to Inadvertent shipment of expired units.
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 Corporation directly.
Affected Products
3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.
Quantity: 2 boxes (5 units per box)
Why Was This Recalled?
Inadvertent shipment of expired units.
Where Was This Sold?
US distribution to Massachusetts only..
About Stryker Corporation
Stryker Corporation has 108 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report