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Stryker Instruments Div. of Stryker Corporation recalls Stryker SmartLife Large Aseptic Housing (7126-120-000)
Recalled May 3, 2017 · FDA recall Z-1886-2017 · Stryker Instruments Div. of Stryker
Hazard
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. · FDA Class II
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302
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Domestic: None Foreign: France, Germany
Description
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.
Product
Stryker SmartLife Large Aseptic Housing (7126-120-000)
Manufacturer(s)
Stryker Instruments Div. of Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →