Vortex Surgical recalls

Vortex Surgical has 15 recalls on record with the FDA and USDA, the earliest in 2024 and the latest reported on 11 Feb 2026. 14 are still ongoing. 14 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls15since 2024

Last 12 months14reported

Class I00% of total

Ongoing14latest 11 Feb 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 1 13Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 15 100%Class III 0 0%

Why vortex surgical is recalled

Sterility1280%
Other Reasons320%

Product types

By year

20261493%
202417%

Ongoing vortex surgical recalls

14 active

Reported	Class	Recall	Company	Reason	Where
11 Feb 2026Device	CLASS II	Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recalled	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Rumex Disposable Diamond Dusted ILM Elevator recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Volk Single Use Vitrectomy Lenses Flat Vitrectomy Lens recalled	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Vortex Disposable Forceps and Cannula recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Subretinal Injection Cannula VS0220.25 recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Tecfen Retractable Membrane Polisher, QTPR1267 recalled	Vortex Surgical	Sterility	Nationwide

All vortex surgical recalls, newest first

15 total

Reported	Class	Recall	Company	Reason	Where
11 Feb 2026Device	CLASS II	Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recalled	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Rumex Disposable Diamond Dusted ILM Elevator recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Volk Single Use Vitrectomy Lenses Flat Vitrectomy Lens recalled	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Vortex Disposable Forceps and Cannula recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Subretinal Injection Cannula VS0220.25 recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Tecfen Retractable Membrane Polisher, QTPR1267 recalled	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	I.D.D. Internal Delivery Device, VS0250.25 recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Oertli 1. Laser Probe OS4 Flex-Tip VK401113 2. Laser Probe recalled	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Backflush, VS0270.25 recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	I2 Injection Kit, VS0500 recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	TID Pharos Illuminated Depressor, VS0801B recalled by Vortex Surgical	Vortex Surgical	Other	Nationwide
11 Feb 2026Device	CLASS II	1. Laser Probe Curved recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
11 Feb 2026Device	CLASS II	Convenience Kits recalled by Vortex Surgical	Vortex Surgical	Sterility	Nationwide
7 Jan 2026Device	CLASS II	Illuminated Flex-Tip Laser Probe recalled by Vortex Surgical	Vortex Surgical	Other	MO
7 Feb 2024Device	CLASS II	Actu8 Forceps, Adaptive recalled by Vortex Surgical	Vortex Surgical	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.