Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe recall
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Why was Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe recalled?
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040
- Product
- Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
- Recalling firm
- Vortex Surgical Inc.
- Quantity
- 221 units
- Distribution
- US and Japan
- Recall date
- January 7, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)