Cataract lens recall is yours on the List

I only check the Abbott lens , you will have to go to the FDA web site  and ches yours

intraocular lens24 - Product Code HQL25

Product ReSTOR intraocular lens and ReSTOR Toric intraocular lens.

The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular lenses are posterior chamber lenses intended as optical implants designed to replace the human crystalline lens in adult patients following cataract surgery. The lenses subject to this correction are manufactured specifically for Japan.

Code Information Model Numbers: SN6AD1, SN6AD3, SV25T0, MN6AD1,SND1T3, SND1T4, SND1T5 and SND1T6 and all lot numbers.

read Alcon's press release put out in October  

- read the recall notice

Alcon Recalls More AcrySof Intraocular Lenses in Japan

If you suffered complications after ICL surgery, we invite you to join the discussion on FaceBook

IMPORTANT: If you experienced problems related to implantable contact lenses, the FDA wants to hear from you. File a MedWatch report with the FDA online. Alternatively, you may call FDA at 1-800-FDA-1088 to report by telephone, or download a copy of the paper form and either fax it to 1-800-FDA-0178 or mail it using the postage-paid addressed form. Read implantable lens injury reports filed with the FDA (enter product code MTA, select a date range, and click search).

Please note that the ICL is an implantable lens for phakic eyes (those that still have their natural lens).  This is a different category of lens than an IOL (a replacement lens implanted during cataract surgery, after removal of the natural lens).

hi, which Abbott lenses did you check?  thank you, 

FDA  Z9002 I check my model but you an go to the web site and type in your model and name .a list of serial numbers will come up.