Recall Z-1254-2026— Vortex Surgical Inc.

Name: FDA recall Z-1254-2026
Creator: U.S. Food and Drug Administration
Published: 2025-12-16

Class II · Ongoing

Class II FDA medical device recall by Vortex Surgical Inc., initiated 2025-12-16. FDA's recall record names no specific 510(k) clearance for this event. Product: Vortex Surgical TID Pharos Illuminated Depressor, VS0801B. Reason: XXX.

Recalling firm: Vortex Surgical Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-12-16
Firm location: Saint Charles, MO, United States

Product description

Vortex Surgical TID Pharos Illuminated Depressor, VS0801B

Reason for recall

XXX

Data sourced from openFDA. This site is unofficial and independent of the FDA.