Beaver Visitec International, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1200-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

CustomEyes kits

Product Classification:

Class II

Date Initiated: December 20, 2022

Date Posted: March 8, 2023

Recall Number: Z-1200-2023

Event ID: 91488

Reason for Recall:

Device packaging may contain open seals, compromising product sterility.

Status: Ongoing

Product Quantity: 4640 units in total

Code Information:

Catalog #BVI-58001086 and BVI-58001089, Lot Numbers 6051841, 6052299, 6051842, 6052300 UDI/DI: 50886158021990 and 50886158021969

Distribution Pattern:

US distribution in AL, CA, CO, DC, FL, GA, IL, LA, MD, MN, MT, NC, NH, NJ, NM, NY, OH OK, PA, RI, TN, TX, UT, VA, VT, WA, and WI OUS distribution to Canada, Japan, and South Africa

Voluntary or Mandated:

Voluntary: Firm initiated