Focus * DAILIES * Toric * One-Day Contact Lenses * CIBA Vision
FDA Recall Z-1402-06 · Posted 2006-08-16
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Recalling FirmCiba Vision Corporation
Recall StatusTerminated
Product CodeLPL
Date Initiated2006-07-25
Date Terminated2006-12-27
Product Quantity86 (approx 1000 lenses) packs total
Reason for Recall
Misbranding; Lenses (-0.75) are labeled with the incorrect power of (-1.50) .
Firm Action
Consignees were notified by letter on/about 07/25/06 to return any of the affected lots found in inventory
Root Cause
Other
Distribution Pattern
Nationwide including the states of CA, HI, IL, MA, MI, NE, NJ, NY, OH, TX, UT, VA, WA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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