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U.S. Department of Health and Human Services

Class 2 Device Recall CSI Daily wear

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  Class 2 Device Recall CSI Daily wear see related information
Date Initiated by Firm September 13, 2006
Date Posted November 04, 2006
Recall Status1 Terminated 3 on February 28, 2009
Recall Number Z-0018-07
Recall Event ID 36382
Product Classification Contact lenses - Product Code LPL
Product CSI¿ Daily Wear, soft (hydrophilic) contact lenses
Code Information Polymer Lot #RM-309824, RM-309691, RM-309631, RM-309592, 03D0201, 03D1401, RM-309825, RM-309762
Recalling Firm/
Manufacturer		 Ciba Vision Corporation
11460 Johns Creek Pkwy
Duluth GA 30097-1518
For Additional Information Contact Gina Ingraham
678-415-4088
Manufacturer Reason
for Recall		 Out of specification lens curve
FDA Determined
Cause 2		 Other
Action Consignees were notified via traceable mail on 09/13/2006.
Quantity in Commerce 42,075 units
Distribution Worldwide-U.S., Canada, Australia and Barbados.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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