Vascular Solutions, Inc Vari-Lase Endovenous Laser Procedural Kit, Model 7000 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vari-Lase Endovenous Laser Procedural Kit, Model 7000
Brand
Vascular Solutions, Inc
Lot Codes / Batch Numbers
Lot numbers S000102, 300537, and 300536.
Products Sold
Lot numbers S000102, 300537, and 300536.
Vascular Solutions, Inc is recalling Vari-Lase Endovenous Laser Procedural Kit, Model 7000 due to An internal gasket of the Fiber Lock component of the Vari-Lase Kit contains natural rubber latex, but the product labeling does not recognize the pr. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An internal gasket of the Fiber Lock component of the Vari-Lase Kit contains natural rubber latex, but the product labeling does not recognize the presence of latex and include the required cautionary statement.
Recommended Action
Per FDA guidance
Letters dated October 9, 2003 were sent to the consignees. The letters instruct the consignees to place the enclosed warning stickers, about latex in the product, on the boxes and pouches of any remaining product in inventory at the consignees. After completing the relabeling, consignees are to fill out the attached form and fax it to the firm to document the field correction.
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