Beaver-Visitec International Inc.: Medical Device Recall in 2015 - (Recall #: Z-1803-2015)

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: 584648 Ophthalmic surgical kits

Product Classification:

Class II

Date Initiated: May 1, 2015

Date Posted: June 24, 2015

Recall Number: Z-1803-2015

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: 384 kits

Code Information:

Lot Numbers: 3038787 3046210 3061080 3078492 3093681 3095940 3108668

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated