Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason for the voluntary recall is residue was...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Vortex Surgical Inc. directly.
Affected Products
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Quantity: 800 devices
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Vortex Surgical Inc.
Vortex Surgical Inc. has 15 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report