Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments Div. of Stryker Corporation Due to The firm received complaints regarding insufficient irrigation to...
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 Instruments Div. of Stryker Corporation directly.
Affected Products
Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
Quantity: 2,460 units
Why Was This Recalled?
The firm received complaints regarding insufficient irrigation to the tip of the Sonopet system. Lack of irrigation can potentially lead to excessive heat at the tip.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Instruments Div. of Stryker Corporation
Stryker Instruments Div. of Stryker Corporation has 161 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report