Cataract lens recall is yours on the List
Posted , 4 users are following.
Check FDA to see if your ser number is on the recall list. I had my Lens company called me to ask for my ser number, If a company has several lens recall why would I want this product in my eye.
cataract surgeny is a billion dollars business.
This your eyesight we are talking about not a store return.
Do a lot of research... go to FB type in Negative Dysphotopsia.
Doctors recieve what is called samplers and you are the guinea pig
if your doctor selects you to inplant the samplers.
0 likes, 10 replies
joe12790 cuz4concern
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cuz4concern joe12790
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cuz4concern joe12790
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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.
cuz4concern
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read Alcon's press release put out in October
- read the recall notice
cuz4concern
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cuz4concern
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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).
rgCalifornia cuz4concern
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joy78503 cuz4concern
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cuz4concern joy78503
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joe12790 cuz4concern
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