Beaver-Visitec International Inc.: Medical Device Recall in 2015 - (Recall #: Z-1802-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic surgical kits

Product Classification:

Class II

Date Initiated: May 1, 2015

Date Posted: June 24, 2015

Recall Number: Z-1802-2015

Event ID: 71293

Reason for Recall:

Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product

Status: Terminated

Product Quantity: 621 kits

Code Information:

Lot Numbers: 3035614 3046205 3052693 3055885 3063181 3068806 3073917 3082315

Distribution Pattern:

Nationwide Distribution including KY, GA, MI, and NJ.

Voluntary or Mandated:

Voluntary: Firm initiated