Beaver Visitec International, Inc. CustomEyes kits Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CustomEyes kits
Brand
Beaver Visitec International, Inc.
Lot Codes / Batch Numbers
Catalog #BVI-58001086 and BVI-58001089, Lot Numbers 6051841, 6052299, 6051842, 6052300 UDI/DI: 50886158021990 and 50886158021969
Products Sold
Catalog #BVI-58001086 and BVI-58001089, Lot Numbers 6051841, 6052299, 6051842, 6052300 UDI/DI: 50886158021990 and 50886158021969
Beaver Visitec International, Inc. is recalling CustomEyes kits due to Device packaging may contain open seals, compromising product sterility.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device packaging may contain open seals, compromising product sterility.
Recommended Action
Per FDA guidance
A consignee letter was issued to impacted customers on January 18, 2023. The communication advises consignees to immediately examine inventory and quarantine product from impacted lots. If further distribution has occurred, a sub-recall should be initiated. A completed copy of the Business Response Form shall be completed and returned to beavervisitec8978@sedgwick.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, CA, CO, FL, GA, IL, IN, LA, MD, MN, MT, NH, NJ, NM, NY, NC, OH, OK, PA, RI, TN, TX, UT, VT, VA, WA, WI, DC
Page updated: Jan 10, 2026