Stryker Medical Div. of Stryker Corporation Stryker inTouch Critical Care bed; Model 2130, Stryker Medical, Portage, MI 49002 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker inTouch Critical Care bed; Model 2130, Stryker Medical, Portage, MI 49002
Brand
Stryker Medical Div. of Stryker Corporation
Lot Codes / Batch Numbers
All units (Model Number 2130/Serial Numbers: T01145 thru T01156, T01335 thru T01348 and TO1160 thru T01168)
Products Sold
All units (Model Number 2130/Serial Numbers: T01145 thru T01156, T01335 thru T01348 and TO1160 thru T01168)
Stryker Medical Div. of Stryker Corporation is recalling Stryker inTouch Critical Care bed; Model 2130, Stryker Medical, Portage, MI 49002 due to Multiple defects: 1) beds exhibit reverse motions when the Fowler, gatch or foot section is activated 2) a battery charging defect which may result i. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Multiple defects: 1) beds exhibit reverse motions when the Fowler, gatch or foot section is activated 2) a battery charging defect which may result in a depletion of battery power 3) the touch screen on the footboard freezing, resulting in controls to powered, pressure-relief mattresses being difficult to access 4) beds equipped with zoom drive systems may have an overdrive problem which could re
Recommended Action
Per FDA guidance
Consignees were notified via an Urgent Medical Device Correction letter dated 11/2/07, and instructed to remove the beds from service if they display any unintended motions and informed that one of the firm's field service representatives will visit the facility to make corrections to all beds under recall.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026