ProClear Toric contact lenses are made from a material containing 62% water and 38% omafilcon B, a random copolymer of 2-hydroxyethylmethacrylate and methacrylic acid. The lenses have a tint (VAT Blue 6) which is added to make the lens more visible for handling.
FDA Recall Z-0134-2015 · Posted 2014-10-24
Recalling FirmCooper Vision Caribbean Corp.
Recall StatusTerminated
Product CodeLPL
Date Initiated2014-09-17
Date Terminated2015-06-10
Product Quantity13639 lenses/246 product lots
Reason for Recall
Routine quality monitoring system has identified that a limited
number of lots were manufactured with the cylinder axis outside the allowable specification.
Firm Action
The firm sent out a notification letter with the following instructions:
Please take the following actions immediately:
" Examine your inventory for any affected lot numbers
o Use the enclosed report to inspect your inventory for affected product that is still in your
Warehouse.
" Stop any further distribution of the specified lots of Preclear T oric lenses.
" Quarantine any Preclear Toric lenses with the specified lot numbers.
" Within the next five (5) business days, please complete the attached Recall Response Form and
fax it to 866-484-1048 or scan and email to [email protected].
o If you have indicated that you have product to return, you will be contacted by a
CooperVision Representative with instructions for pick-up and removal of affected,
quarantined product. Your account will be credited once the product is returned and
processed.
This action is being taken in full cooperation with the Food and Drug Administration (FDA). The recall only
affects Proclear T oric lenses with the lot numbers specified on the enclosed list. No other Preclear T oric
products- or any other CooperVision products - are affected.
Root Cause
Other
Distribution Pattern
Worldwide Distribution: US (nationwide) and internationally to: Canada, Latin America, EU, Asia Pacific, and Africa/Central Eurasia countries.
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.