Beaver Visitec: Medical Device Recall in 2018 - (Recall #: Z-2342-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 14, 2018

Date Posted: July 11, 2018

Recall Number: Z-2342-2018

Event ID: 80311

Reason for Recall:

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

Status: Terminated

Product Quantity: 1354 units

Code Information:

Lot Numbers: 6002436 & 6002663

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated