Bausch & Lomb Surgical, Inc. recalls
8 recalls in our records from 2014 to 2025: 8 FDA medical devices.
Recalls with full detail pages
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Bausch & Lomb Surgical, Inc. medical device recall: Intraocular lens. enVista Monofocal IOL
In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and…
Earlier and other recalls
These link to the official agency notice.
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Bausch & Lomb Surgical, Inc. medical device recall: Akreos Official notice ↗
An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in…
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Bausch & Lomb Surgical, Inc. medical device recall: Mx60Et Official notice ↗
Product may be missing toric axis marks.
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Bausch & Lomb Surgical, Inc. medical device recall: enVista one-piece hydrophobic acrylic toric intraocular lens Official notice ↗
The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens.
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Bausch & Lomb Surgical, Inc. medical device recall: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated… Official notice ↗
Cosmetic imperfections on the surface of some lenses.
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Bausch & Lomb Surgical, Inc. medical device recall: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the… Official notice ↗
Complaints concerning kinked haptics that were occurring during lens delivery.
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Bausch & Lomb Surgical, Inc. medical device recall: Bausch & Lomb SofPort Advanced Optics Aspheric Lens Official notice ↗
Haptics breaking during lens loading and insertion.
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Bausch & Lomb Surgical, Inc. medical device recall: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended… Official notice ↗
Lens was manufactured with incorrect raw material.
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.