Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Veritas Advanced Infusion Packs. Used in ophthalmic procedures. Recalled by Johnson & Johnson Surgical Vision, Inc. Due to As a result of returned product complaints for...
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 Johnson & Johnson Surgical Vision, Inc. directly.
Affected Products
Veritas Advanced Infusion Packs. Used in ophthalmic procedures.
Quantity: 53,624 units
Why Was This Recalled?
As a result of returned product complaints for Veritas Phaco packs related to broken or cracked irrigation luer due to a manufacturing issue.
Where Was This Sold?
This product was distributed to 25 states: AL, AZ, AR, CA, CO, DE, FL, GA, HI, IL, IN, KY, LA, MN, MS, MO, NJ, NY, NC, OH, TN, TX, UT, VA, WA
About Johnson & Johnson Surgical Vision, Inc.
Johnson & Johnson Surgical Vision, Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report