Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker SmartLife Large Aseptic Housing (7126-120-000) Recalled by Stryker Instruments Div. of Stryker Corporation Due to Stryker Instruments issued a notice of correction for...
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
Stryker SmartLife Large Aseptic Housing (7126-120-000)
Quantity: 302
Why Was This Recalled?
Stryker Instruments issued a notice of correction for an update to cleaning practices for the Stryker SmartLife Large Aseptic Housings following complaints of deterioration to the housing and the top and bottom housing separating at the weld. Using cleaning practices outside of the HIFU could lead to housing separating at the weld.
Where Was This Sold?
Domestic: None Foreign: France, Germany
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