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Beaver Visitec recalls Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surger
Recalled July 11, 2018 · FDA recall Z-2342-2018 · Beaver Visitec
Hazard
Blades are loose in handles and may fall out due to non cured epoxy · FDA Class II
Units
1354 units
Sold at
US Nationwide in the states of CA, IA, CO, HI, IA, MD & TX
Description
Blades are loose in handles and may fall out due to non cured epoxy
Product
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Manufacturer(s)
Beaver Visitec
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →