Beaver Visitec International, Inc. is recalling approximately 38,878 BVI CustomEyes Procedure Packs because they contain 1ml syringes manufactured by Sol-Millennium Medical (Sol-M) that were previously recalled. These kits include various combinations of Sol-M Luer Lock and Luer Slip tip syringes used in medical procedures. The recall was initiated following a voluntary recall by the original syringe manufacturer regarding potential defects in low dead space and slip tip syringe designs.
Defective syringes can lead to inaccurate medication dosing or mechanical failure during medical procedures, potentially resulting in patient harm or delays in treatment. No specific injuries have been reported in this notice, but the syringe manufacturer identified risks that led to the primary recall of these components.
Quarantine and Return affected procedure packs
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.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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.