Recall Z-2161-2024— Beaver Visitec International, Inc.

Name: FDA recall Z-2161-2024
Creator: U.S. Food and Drug Administration
Published: 2024-05-10

Class II · Ongoing

Class II FDA medical device recall by Beaver Visitec International, Inc., initiated 2024-05-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227. Reason: The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down)..

Recalling firm: Beaver Visitec International, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2024-05-10
Firm location: Waltham, MA, United States

Product description

Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227

Reason for recall

The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).

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