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All product recalls associated with Bausch & Lomb Inc.
Total Recalls
40
Past Year
3
Class I (Serious)
0
Most Recent
Jun 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
During routine testing the product failed to meet shelf life specifications.
The product failed to meet one of the shelf life specifications at the end of the expiry period.
Affected lenses were inadvertently shipped to Bausch & Lomb's European Logistics Center (ELC) prior to release authorization. Initial testing indicated the product did not meet release criteria for endotoxin limits.