Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Recalled by Stryker Corporation Due to Complaints were received for the Stryker FlowPort II...
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
Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Adapter is intended to connect the FlowPort II Cannulas to commercially available, 4mm arthroscopes in surgical procedures.
Quantity: 21 units
Why Was This Recalled?
Complaints were received for the Stryker FlowPort II Adapter, and investigation found that the scope sat in the adapter 180 degrees in the wrong direction
Where Was This Sold?
This product was distributed to 5 states: GA, MD, MT, NJ, UT
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