Reported Jan 22, 2025 · Ongoing

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

Alcon Research LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Alcon Research LLC · 6201 South Fwy · Fort Worth, TX · 76134-2099

Is this the product you have?

  • Brand NameAlcon
  • Product NameMonarch¿ III D
  • Delivery Cartridge Model/Catalog Number8065977763
  • Product DescriptionMonarch¿ III D delivery cartridge Lens Guide
  • Intraocular ComponentN/A
Lot codes and dates
  • GTIN/UDI 10380659777636/ Lot #

    336 of 336 codes

    • 15895927
    • 15895928
    • 15895929
    • 15895930
    • 15895931
    • 15895932
    • 15895933
    • 15895934
    • 15895935
    • 15895936
    • 15895937
    • 15895938
    • 15895939
    • 15895940
    • 15895941
    • 15895942
    • 15895965
    • 15895969
    • 15895973
    • 15895977
    • 15899643
    • 15899644
    • 15899687
    • 15899688
    • 15899689
    • 15899690
    • 15899691
    • 15899692
    • 15899693
    • 15899695
    • 15899696
    • 15899697
    • 15899698
    • 15899700
    • 15899701
    • 15899730
    • 15899731
    • 15899732
    • 15899733
    • 15899734
    • 15899735
    • 15899736
    • 15899737
    • 15899738
    • 15899753
    • 15904026
    • 15904027
    • 15904028
    • 15904029
    • 15904030
    • 15904031
    • 15904032
    • 15904033
    • 15904034
    • 15904035
    • 15904036
    • 15904037
    • 15904038
    • 15904039
    • 15904040
Amount recalled
41718 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

Increase in complaints associated with a molding defect within the inner lumen of delivery cartridges which could result in a scratch on the intraocular lens (IOL) upon delivery.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.