Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SHIMADZU MobileDaRt Evolution (MX8 Version) Recalled by Shimadzu Medical Systems Usa Com Due to In these units, the brake is usually released...
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 Shimadzu Medical Systems Usa Com directly.
Affected Products
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR).
Quantity: 93 units
Why Was This Recalled?
In these units, the brake is usually released by gripping the drive handle and applied by letting go of the handle. However, for systems within a specified manufacture period, we have identified that even when letting go of the handle, the systems brakes are not applied. In this event, if the Operator releases the handle when the device is moving, the unit will continue to coast.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Shimadzu Medical Systems Usa Com
Shimadzu Medical Systems Usa Com has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report