Vortex Surgical Inc.: Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Read the official notice at FDA (device) →
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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Vortex Surgical Inc.
- Product
- Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
- Reason / hazard
- Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- US and Japan
- Recall initiated
- 2025-11-19
- Code info
- UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040
- Product quantity
- 221 units
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Saint Charles
- State
- MO
- Country
- United States
- Event id
- 98032
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