Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical Division of Stryker Corporation Due to An adverse trend of scale and bed exit...
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 Medical Division of Stryker Corporation directly.
Affected Products
Go Bed II+ Model FL 28 Ex Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
Quantity: 9440
Why Was This Recalled?
An adverse trend of scale and bed exit service reports/complaints were detected for the GoBed+, GoBed II, Rose, and MA204 model beds. Investigation found an abnormally high failure rate of loadcells, an integral component in scale and bed exit function. The scale faults are manifested as a fluctuating scale reading, a scale error causing the scale system to be disabled until serviced, or an inac
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Medical Division of Stryker Corporation
Stryker Medical Division of Stryker Corporation has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report