PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: February 7, 2018 Initiated: November 3, 2017 #Z-0501-2018

Product Description

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.

Reason for Recall

The protective shield was retracted, and the blade was exposed.

Details

Units Affected
572,490 units
Distribution
Worldwide Distribution - US Nationwide and the countries of Italy, UK, Finland, Germany, Ireland, Turkey
Location
Waltham, MA

Frequently Asked Questions

What product was recalled?
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.. Recalled by Beaver-Visitec International Inc.. Units affected: 572,490 units.
Why was this product recalled?
The protective shield was retracted, and the blade was exposed.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 7, 2018. Severity: Moderate. Recall number: Z-0501-2018.