We collected information about Alcon Laboratories Fda Complaints for you. There are links where you can find everything you need to know about Alcon Laboratories Fda Complaints.
https://www.alcon.com/contact-us
Contact Alcon with any product quality concerns or to report a question. Alcon welcomes your feedback to continue driving us as the global leader in eye care. Go to main content. ... To report product complaints or adverse events from the US please call 1 800 757 9780.
Our mission is to provide innovative vision products that enhance quality of life by helping people see better. From vision research to eye health, learn more at Alcon.com.
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=2743875
There have been no other complaints reported in the lot number. Attempts have been made to obtain additional info; however, the surgeon was unwilling to provide any additional info. (b)(4).
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=2739341
MAUDE Adverse Event Report: ALCON - FORT WORTH/ALCON LABORATORIES INC. ALCON CONTACT LENS CASE. FDA Home; Medical Devices; Databases - 510(k) ... Review of the complaint history for the lens case lots mf02007 and mf02009 showed no other complaints were reported. ... Date FDA Received: 09/07/2012: Is This An Adverse Event Report? ...
Open your eyes to a new world and learn about products and resources for consumers and eyecare professionals alike. Find out more at MyAlcon today!
https://www.fiercebiotech.com/medical-devices/updated-novartis-alcon-recalling-more-intraocular-lenses-japan-due-to-reports
Nov 30, 2015 · Novartis' Alcon expanded the recall of its intraocular lenses in Japan, pushing the number of affected units to 89,042, due to a continued increase in reports of postoperative inflammation among ...
https://www.myalcon.com/professional/cataract-surgery/intraocular-lens/acrysof-iq-monofocal-iol
WARNINGS/PRECAUTIONS: Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting an IOL in a patient with any of the conditions described in the Directions for Use that accompany each IOL. Caution should be used prior to lens encapsulation to avoid lens decentration or dislocation.
https://www.drugs.com/fda-alerts/1740-9422.html
Jul 16, 2019 · Systane FDA Alerts. The FDA Alert(s) below may be specifically about Systane or relate to a group or class of drugs which include Systane (ocular lubricant). MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. Following is a list of possible medication recalls, market withdrawals, alerts and warnings.
https://www.myalcon.com/professional/cataract-surgery/intraocular-lens/acrysof-iq-monofocal-iol/monofocal-iol-specifications
INDICATIONS: AcrySof ® single-piece monofocal intraocular lenses (IOLs) include the AcrySof ® IQ Aspheric Natural IOL (Model SN60WF), AcrySof ® UV-Absorbing Aspheric IOL (Model SA60WF), AcrySof ® Natural IOL (Model SN60AT) and AcrySof ® IOL (Model SA60AT). Each IOL is indicated for visual correction of aphakia in adult patients following cataract surgery
https://www.hipaaspace.com/Medical_Billing/Coding/Global.Unique.Medical.Device.Identification/00380652332385
Global Unique Device ID: 00380652332385. Version (Model) Number: SA60WF. Device Name: AcrySof(R) ASPHERIC IOL, SINGLE-PIECE ACRYLICFOLDABLE POSTERIOR CHAMBER LENS,UV-ABSORBING, 13.0mm LENGTH, 6.0mm ANTERIORASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.. Company Name: Alcon Laboratories, Inc.. Brand Name: ACRYSOF®.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843900/
Nov 08, 2013 · Materials and Methods. In the cases reported here, the patients received a blue light-filtering IOL (AcrySof IQ Natural SN60WF; Alcon Laboratories, Fort Worth, Tex., USA) in their first operated eye followed by implantation of a non-blue light-filtering IOL in their second eye (Tecnis 1-Piece IOL; Abbott Medical Optics, Santa Ana, Calif., USA).
https://www.drugs.com/disease-interactions/bimatoprost-ophthalmic,lumigan.html
Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Data sources include IBM Watson Micromedex (updated 3 Feb 2020), Cerner Multum™ (updated 5 Feb 2020), Wolters Kluwer™ (updated ...4.7/10
https://96bda424cfcc34d9dd1a-0a7f10f87519dba22d2dbc6233a731e5.ssl.cf2.rackcdn.com/metroplex/Lessons_Learned_in_Resolving_FDA_Warning_Letters_-_Distributable.pdf
Lessons Learned in Resolving FDA Warning Letters In this presentation, Mark Neal, VP Global Quality Systems and Assurance at St. Jude Medical, will describe his experience and lessons learned from numerous FDA inspections and specifically his work to clear five Warning Letters in four FDA Districts.
https://caselaw.findlaw.com/us-3rd-circuit/1877352.html
ALCON LABORATORIES RP USA LLC LLC. Read the Court's full decision on FindLaw. ... since they could not simultaneously comply with FDA requirements and with state consumer protection laws that ... “reluctance to endorse standing theories that rest on speculation about the decisions of independent actors.” 9 Complaints alleging such abstract ...
https://www.medscape.com/viewarticle/838769
Nov 05, 2019 · Dr Waltz is a consultant for, and all other authors are employees of, Abbott Medical Optics Inc. Dr Miller works with Alcon Laboratories. Ophthalmology . Published online …
https://www.cataractsurgerycost.net/iols-intraocular-lenses/
2. Acrysof monofocal lens implant: The Acrysof monofocal lens implant is produced by Alcon Laboratories. The normal human crystalline lens has the ability to filter the high energy blue light in order not to cause harmful impacts on the delicate retina as a …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039401/
May 22, 2014 · Long-term visual outcomes after Crystalens ® HD intraocular lens implantation. ... Our purpose was to evaluate the long-term visual outcomes after bilateral implantation of Crystalens ... All eyes also received cyclopentolate 1% (Cyclogyl ®; Alcon Laboratories, Inc.) twice daily for 5 days in order to assure the posterior lens position.19.Cited by: 3
https://www.medhelp.org/posts/Eye-Care/class-action/show/796958
I feel like I am in a fog and cannot think clear! The ReSTOR Mulit focal lens in question are on file with the FDA, the recall is number Z-2323-2015, I found this on my own, my eye doctor acted like he knew nothing about the recall! I understand the FDA require Alcon Laboratories makers of the lens to notify the doctors that used these model ...
https://www.fda.gov/safety/enforcement-reports/pending-recalls
Pending Recalls. UPDATE: In July 2011, FDA began a pilot program to notify people of drug recalls before they are classified in an effort to expedite notifications of human drug product recalls to ...
Searching for Alcon Laboratories Fda Complaints information?
To find needed information please click on the links to visit sites with more detailed data.
