Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Ca... (Vortex Surgical Inc.) – reason for the voluntary recall is so... (2025)
Surgical probe may not smoothly pass through medical cannula during procedures.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Brand
Vortex Surgical Inc.
Lot Codes / Batch Numbers
UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040
Products Sold
UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040
Vortex Surgical Inc. is recalling Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25; due to Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Recommended Action
Per FDA guidance
Vortex Surgical Inc. issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 11/19/2025 via email. The notice explained the issue, risk to health, and requested the use of the product be discontinued. The firm requested the response to be emailed to: ARitts@VortexSurgical.com for replacement or refund. Customer Service will provide a return label for any unused products.
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