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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Beaver Visitec International, Inc.: Device packaging may contain open seals, compromising product sterility.

Agency Publication Date: March 1, 2023
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Affected Products

Product: Ultracell Wick with 80cc Collection Bag, 20/box

Catalog #40430, Lot Numbers 21M3820 and 21L3403 UDI/DI: 30886158012123

Lot Numbers:
Numbers
Product: CustomEyes kits

Catalog #BVI-58001086 and BVI-58001089, Lot Numbers 6051841, 6052299, 6051842, 6052300 UDI/DI: 50886158021990 and 50886158021969

Lot Numbers:
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91488
Status: Active
Manufacturer: Beaver Visitec International, Inc.
Manufactured In: United States
Units Affected: 2 products (4640 units in total)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.