Candela Laser Corporation Candela Laser VBeam Perfecta, a Pulsed Dye Laser used for General Surgery, Dermatology, Gynecology, Podiatry. Model Number: 9914-00-0300 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Candela Laser VBeam Perfecta, a Pulsed Dye Laser used for General Surgery, Dermatology, Gynecology, Podiatry. Model Number: 9914-00-0300
Brand
Candela Laser Corporation
Lot Codes / Batch Numbers
Serial Number: SN 9998, 9914-0300-0001 through 9914-0300-0058
Products Sold
Serial Number: SN 9998; 9914-0300-0001 through 9914-0300-0058
Candela Laser Corporation is recalling Candela Laser VBeam Perfecta, a Pulsed Dye Laser used for General Surgery, Dermatology, Gynecology, due to Handle fires even when the finger is off the switch. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Handle fires even when the finger is off the switch
Recommended Action
Per FDA guidance
Candela notified Service Representaives by email on 1/17/06 providing Technical Service Bulletin, listing of laser systems to be reworked and script to address customer questions during visit to correct system.
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