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Vortex Surgical Inc.

Vortex Surgical Inc. Recalls

All product recalls associated with Vortex Surgical Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–2 of 2 recalls

Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Ca... (Vortex Surgical Inc.) – reason for the voluntary recall is so... (2025)

Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.

Moderate

FDANov 19, 2025Nationwide• Vortex Surgical Inc.

ACTU8 Forceps (Vortex Surgical) – Residue Contamination (2023)

Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.

Moderate

FDADec 18, 2023Nationwide• Vortex Surgical Inc.