Vision Systems Group, A Div of Viking Systems Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite Xenon, Model 8050-1 and Boston Scientific Spyglass 300W Light Source (M00546190) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite Xenon, Model 8050-1 and Boston Scientific Spyglass 300W Light Source (M00546190)
Brand
Vision Systems Group, A Div of Viking Systems
Lot Codes / Batch Numbers
Units manufactured from 1/23/07 through 3/14/07 with serial numbers: 120906, 016707, 016907, 017007
Products Sold
Units manufactured from 1/23/07 through 3/14/07 with serial numbers: 120906, 016707, 016907, 017007
Vision Systems Group, A Div of Viking Systems is recalling Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite Xenon, Model 8050-1 a due to Incorrect power entry module assembled into unit may cause burning to insulation, compromised electrical emissions and premature light source failure. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect power entry module assembled into unit may cause burning to insulation, compromised electrical emissions and premature light source failure
Recommended Action
Per FDA guidance
Viking notified 2 distributors and 1 end user by telephone on 3/15/07. Viking representatives performed on site visit to perform inspection and replace units if needed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026