Philips Medical Systems (Cleveland) Inc recalls BrightView XCT , Model Number 882482
- Recall date
- June 10, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2011-2019
- FDA classification
- Class II
- Brand / firm
- Philips Medical Systems (Cleveland) Inc
- Sold / distributed
- Worldwide Distribution - US Nationwide
Why it was recalled
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
BrightView XCT , Model Number 882482
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