Beaver-Visitec International Inc.: Medical Device Recall in 2015 - (Recall #: Z-1804-2015)

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: 584649 Ophthalmic surgical kits

Product Classification:

Class II

Date Initiated: May 1, 2015

Date Posted: June 24, 2015

Recall Number: Z-1804-2015

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: 585 kits

Code Information:

Lot Numbers: 3039720 3046211 3047770 3049473 3070763 3082330 3089827 3093682 3095941 3106407 3117874

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated