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Devices
Device Recall Stryker inTouch Zoom Critical Care
Model / Serial
All units. (Model Number 2140/Serial Numbers: T01121, T01205, T01350, T01213 thru T01214, T01224, T01014 thru T01036, T01143, T01227, T01211, T01379 thru T01383, T01202, T01053 thru T01099. T01100 thru T01144, T01159, T01179, T01182, T01378, T01186, T01201, T01212, T01057, T01060,T01079,T01200, T01183, T01189, T01223, T01209, T01218, T01172, T01188, T01058, T01171, T01173, T01195, T01203, T01206, T01210, T01216, T01217, T01228, T01176, T01185, TO1193, T01207, T01225, T01215, T01229, T01187, T01311 thru T01320, T01230, T01175, T01180, T01190, T01196, T01037 thru T01052, T01198, T01184, T01192, T01177, T01194, T01204, T01219, T01199, T01191, T01226, T01181, T01197, T01222, T01231 thru T01308,T01208, T01349, T01221, QT01001 thru QT01012, QT01169 and QT01170)
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide-USA and Canada
Product Description
Stryker inTouch Zoom Critical Care bed, Model 2140, Stryker Medical, Portage, MI 49002
Manufacturer
Stryker Medical Div. of Stryker Corporation
1 Event
Recall of Device Recall Stryker inTouch Zoom Critical Care
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Manufacturer
Stryker Medical Div. of Stryker Corporation
Manufacturer Address
Stryker Medical Div. of Stryker Corporation, 3800 E. Centre Ave., Portage MI 49002
Source
USFDA
Language
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