Beaver Visitec recalls Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery

Recall date

May 14, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2342-2018

FDA classification

Class II

Brand / firm

Beaver Visitec

Sold / distributed

US Nationwide in the states of CA, IA, CO, HI, IA, MD & TX

Why it was recalled

Blades are loose in handles and may fall out due to non cured epoxy

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery