Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part Number Recalled by Alcon Research, Ltd. Due to Alcon CUSTOM-PAK which is supposed to contain a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Alcon Research, Ltd. directly.
Affected Products
Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part Number 585006 contained in Alcon Assembly Numbers 9795-37, 11233-14, and 13334-04. The product is typically inserted through an incision during cataract surgery to deliver balanced salt solution to help anterior chamber space and replace fluids that are lost during surgery.
Quantity: 684 total (525 units in US)
Why Was This Recalled?
Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula (27G x 7/8 in) actually contains a 27G Sharp Tip Needle
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alcon Research, Ltd.
Alcon Research, Ltd. has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report