Bausch & Lomb Surgical, Inc. recalls
Every recall we track for Bausch & Lomb Surgical, Inc. — 6 in all, from 2018–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Bausch & Lomb Surgical, Inc. peaked in 2025 (3); 6 since 2017.
All FDA recall records for Bausch & Lomb Surgical, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 2 | 0 | 2 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 1 | 2 | 0 | 3 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Bausch & Lomb Surgical, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Bausch & Lomb Surgical, Inc. recalls
5 shown- Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls Akreos, SKU: AO60P0300. Akreos intraocular lenses
Bausch & Lomb recalls Akreos intraocular lenses (SKU AO60P0300) with a 16 diopter error instead of 3, risking vision impairment. Affected lenses have specific serial numbers and lot codes.
Bausch & LombJun 6, 2025 - Use cautionMedical device
Bausch & Lomb Surgical, Inc. recalls Intraocular Lens. enVista Envy IOL, All models starting with EN; enVista Envy Toric IOL, All models starting with ETN.
Bausch & Lomb recalls enVista Envy IOLs and Toric IOLs starting with EN or ETN models due to reports of toxic anterior segment syndrome (TASS) after implantation. Affected units include specific lot numbers and UDI-DI codes listed in the recall.
Bausch & LombMar 27, 2025 - Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is
Bausch & Lomb recalls MX60ET toric contact lenses due to possible missing toric axis marks. Affected lenses may not fit properly during eye surgery.
Bausch & LombNov 7, 2020 - Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary
Bausch & Lomb recalls enVista one-piece hydrophobic acrylic toric intraocular lenses with misaligned toric axis marks that could affect surgical outcomes after cataract removal.
Bausch & LombJun 9, 2020 - Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual
Bausch & Lomb recalls enVista One Piece Hydrophobic Acrylic Intraocular lenses with cosmetic imperfections on the surface. Affected models include MX60E and specific SKUs from MXUE0000 to MXUE3400.
Bausch & LombNov 5, 2018
Bausch & Lomb Surgical, Inc. recall questions
How many recalls has Bausch & Lomb Surgical, Inc. had?
6 recalls from Bausch & Lomb Surgical, Inc. are on record with U.S. safety agencies, from 2018–2025.
What is the most recent Bausch & Lomb Surgical, Inc. recall?
Bausch & Lomb Surgical, Inc. recalls Akreos, SKU: AO60P0300. Akreos intraocular lenses, dated Jun 6, 2025. Every Bausch & Lomb Surgical, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Bausch & Lomb Surgical, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Bausch & Lomb Surgical, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.