Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec International Inc. Due to The protective shield was retracted, and the blade...

Date: November 3, 2017
Company: Beaver-Visitec International Inc.
Status: Terminated
Source: FDA (Device)

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 Beaver-Visitec International Inc. directly.

Affected Products

bvi Beaver Safety Sideport Knife: (a) 1.0mm, 45o, REF 378210 (b) 1.2mm, 45o, REF 378212 (c) 115mm, 45o, REF 378231 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.

Quantity: 572,490 units

Why Was This Recalled?

The protective shield was retracted, and the blade was exposed.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Beaver-Visitec International Inc.

Beaver-Visitec International Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report