Weitz & Luxenberg is accepting cases for investigation from clients who developed TASS after undergoing cataract surgery and receiving Bausch + Lomb recalled lenses. This recall involves specific models of intraocular lenses. Bausch + Lomb issued a voluntary recall of its enVista Aspire™, enVista Envy™, and certain enVista® Monofocal intraocular lenses (IOL) on April 3, 2025. (1)
The company issued the recall after receiving reports of toxic anterior segment syndrome (TASS). These are the models affected by the Bausch + Lomb enVista IOL recall: (2)
- enVista Monofocal IOL: All models starting with EE.
- enVista Aspire IOL: All models starting with EA.
- enVista Envy IOL: All models starting with EN.
- enVista Monofocal Toric IOL: All models starting with ETE.
- enVista Aspire Toric IOL: All models starting with ETA.
- enVista Envy Toric IOL: All models starting with ETN.
The FDA has not yet classified this recall. However, Bausch + Lomb is urging all surgery patients experiencing eye discomfort to contact their doctor as soon as possible. (3)
Patients Deserve Medical Devices That Are Not Defective
Recall from medical devices indicate that the manufacturers know their products are defective. “Medical device manufacturers have a duty. Their duty is to make sure their products are safe for use. They must function correctly and not cause harm,” states Ellen Relkin, a partner at W&L and chair of our firm’s Drug and Medical Device Litigation group.
“I’ve dedicated my career and life to helping people suffering due to defective medical devices. The medical manufacturers are supposed to improve, not harm, your health.”
TASS After Cataract Surgery
TASS is a very rare complication following cataract surgery. However, it has been observed by clinicians in a concerning number of patients receiving these IOLs, leading to the recall.
This inflammatory condition affects the front of your eye and comes on quickly. TASS generally develops within 12 to 48 hours following eye surgery. (4) (5)
Symptoms of TASS include: (6)
- Pain, swelling, and redness affecting the front of the eye.
- Corneal edema (clouding of the eye due to damaged endothelial cells).
- Increased intraocular pressure that can lead to secondary glaucoma.
- Dilated, irregular, or non-reactive pupil.
If you’ve had cataract surgery with a recalled lens, you may be entitled to compensation. Contact us now for a free legal consultation.
CONTACT US TODAYIntraocular Lenses for Cataract Surgery
This recall is due to intraocular lens implant complications. The recalled product can cause damage to your eye.
IOLs are used to correct a variety of eye conditions. They are clear, artificial implants that replace your natural, but damaged, lenses. These implants are used to improve your vision. (7)
In addition to cataracts, you might receive an intraocular lens during surgery to correct: (8)
- Myopia, nearsightedness.
- Hyperopia, farsightedness.
- Presbyopia, farsightedness due to aging.
- Astigmatism, altered eye shape.
Intraocular lenses are meant to last a lifetime. A successful surgery improves your vision overall. Some people may find they don’t need to wear glasses after undergoing this kind of eye surgery. (9)
W&L Can Help If You Received Defective Bausch + Lomb Lenses
If you or a loved one was diagnosed with TASS after receiving a Bausch + Lomb enVista intraocular lens, you may be able to file a lawsuit. You may be eligible for compensation.
Weitz & Luxenberg can help you find out what you deserve. Our defective medical device attorneys are prepared to help you explore your legal options. We offer a free initial consultation.
W&L is a nationally recognized firm known for its success in leading complex litigation. We urge you to contact us at (917) LAWYERS for more information. If you prefer, you can fill out the form that appears on this page. One of our representatives is standing by to help you.
