SILVER SPRINGS, Md. (WMTV) -- Pro-Med Instruments is recalling the DORO Lucent Headrest System because recent design revisions can prevent the headrest from fitting together properly.
If parts from different revisions are used together, use of this combination may cause serious adverse health consequences or death.
Recalled serial numbers are 1704001, 1704042, 1709001 and 1709096 manufactured between May 4, 2017 to April 5, 2018. There have been 73 devices recalled, according to the FDA.
For more information, the FDA has a statement on their website.