Bausch & Lomb Incorporated
FDA adverse event reports naming Bausch & Lomb Incorporated as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAUSCH & LOMB INCORPORATED.
- Total reports
- 4,461
- Deaths
- 1
- Injuries
- 588
- Malfunctions
- 3,866
Reports per year
Source: FDA adverse event reports by year received, 2006–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Accessories, Soft Lens ProductsLPN2,927
- Intraocular LensHQL1,056
- Unit, PhacofragmentationHQC94
- Lenses, Soft Contact, Daily WearLPL85
- Lenses, Soft Contact, Extended WearLPM75
- Lens, Intraocular, AccommodativeNAA68
- Folders And Injectors, Intraocular Lens (Iol)MSS36
- Lens, Contact, (Disposable)MVN32
- Accessories, Solution, Ultrasonic Cleaners For LensesLYL26
- Lens, Intraocular, Toric OpticsMJP26
Recent recalls
- 2003-10-15TerminatedOther
Microflow Needles, catalog #DP8200, with 0 degree tapering, labeled in part ***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.
- 2003-10-15TerminatedOther
Phaco Needles, catalog #DP8115, with 15 degree needle taper, labeld in part***Non-sterile, Manufactured for Bausch and Lomb, Inc. Rochester, NY 14609***, packaged 6 needles/box.
The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.
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