Beaver Visitec International, Inc. Ultracell Wick with 80cc Collection Bag, 20/box Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ultracell Wick with 80cc Collection Bag, 20/box
Brand
Beaver Visitec International, Inc.
Lot Codes / Batch Numbers
Catalog #40430, Lot Numbers 21M3820 and 21L3403 UDI/DI: 30886158012123
Products Sold
Catalog #40430, Lot Numbers 21M3820 and 21L3403 UDI/DI: 30886158012123
Beaver Visitec International, Inc. is recalling Ultracell Wick with 80cc Collection Bag, 20/box 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