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
158959271589592815895929158959301589593115895932158959331589593415895935158959361589593715895938158959391589594015895941158959421589596515895969158959731589597715899643158996441589968715899688158996891589969015899691158996921589969315899695158996961589969715899698158997001589970115899730158997311589973215899733158997341589973515899736158997371589973815899753159040261590402715904028159040291590403015904031159040321590403315904034159040351590403615904037159040381590403915904040
- GTIN/UDI 10380659777636/ Lot #
- 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.
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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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