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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-0940-2009 - Stryker InTouch 1.0 Critical Care Bed; Model 2130. The device is intended to be used as an Intensive Care Unit bed. 2 02/25/2009 FEI # 1831750
Stryker Medical Div. of Stryker Corporation
Z-0943-2009 - Stryker InTouch 1.0 Zoom Critical Care Bed (Model 2140) with the Integrated PositionPro mattress (Model 2920) option. The device is intended to be used as an Intensive Care Unit bed. 2 02/25/2009 FEI # 1831750
Stryker Medical Div. of Stryker Corporation
Z-0942-2009 - Stryker InTouch 1.0 Critical Care Bed (Model 2130) with the Integrated PositionPro mattress (Model 2920) option. The device is intended to be used as an Intensive Care Unit bed. 2 02/25/2009 FEI # 1831750
Stryker Medical Div. of Stryker Corporation
Z-0941-2009 - Stryker InTouch 1.0 Zoom Critical Care Bed; Model 2140. The device is intended to be used as an Intensive Care Unit bed. 2 02/25/2009 FEI # 1831750
Stryker Medical Div. of Stryker Corporation
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