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Maquet Medical Systems USA recalls Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area or the patient.
Recalled June 18, 2014 · FDA recall Z-1730-2014 · Maquet Medical Systems USA
Hazard
Maquet has identified an issue with the Maquet PowerLED 700 (certain serial numbers). One or several plastic fixation tabs can break, which can cause the ambient light module to partially detach. · FDA Class II
Units
United States 1169 units
Sold at
US Nationwide Distribution.
Description
Maquet has identified an issue with the Maquet PowerLED 700 (certain serial numbers). One or several plastic fixation tabs can break, which can cause the ambient light module to partially detach.
Product
Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area or the patient.
Manufacturer(s)
Maquet Medical Systems USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →