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Terminated

CSI Daily Wear, soft (hydrophilic) contact lenses

FDA Recall Z-0018-07 · Posted 2006-11-04

Recalling FirmCiba Vision Corporation
Recall StatusTerminated
Product CodeLPL
Date Initiated2006-09-13
Date Terminated2009-02-28
Product Quantity42,075 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.

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