Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

CSI Toric, soft (hydrophilic) contact lenses

FDA Recall Z-0020-07 · Posted 2006-11-04

Recall StatusTerminated
Product CodeLPL
Date Initiated2006-09-13
Date Terminated2009-02-28
Product Quantity9,740 units

Reason for Recall

Out of specification lens curve

Firm Action

Consignees were notified via traceable mail on 09/13/2006.

Root Cause

Other

Distribution Pattern

Worldwide-U.S., Canada, Australia and Barbados.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑