Atlas FDA

FreshLook Toric, Daily wear soft (hydrophilic) contact lens, BC: Median, DIA: 14.5, Sterile, SPH -1.50, CYL -0.75, AXIS

FDA device recall Z-0743-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Ciba Vision Corporation
Reason for recall
The lens inside the package does not match the prescription information labeled on the primary package.
Action taken
Consignees were notified by letter on 3/11/2004.
Root cause
Other
Status
Terminated
Product code
LPM
Quantity affected
10/6pk
Distribution
Nationwide, Canada, Latin America, South America, Germany, Thailand and South Africa.
Date initiated
2004-03-11
Date posted
2004-07-20
Date terminated
2005-11-16
Location
Duluth, GA

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.