SURGERY SHADOW LESS LIGHT MARKET ANALYSIS
Product recalls by U.S. Food and Drug Administration (USFDA) due to faulty surgery shadow less lamps and further chances of injuries is expected to affect the growth of surgery shadow less light market. For instance, in June 2018, FDA recalled VOLISTA StandOP Surgical Light manufactured by Maquet SAS firm. The lamps were recalled due to potential light head detachment issue. Improper assembly of the bracket that connects the light head to the axle fork could result in the light head bracket breaking, causing the light head to detach from the arm. Use of such affected device may result in serious injury to patient and/or medical staff if the light head detaches and drops.
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