AMO Puerto Rico MFG. Inc.
FDA adverse event reports naming AMO Puerto Rico MFG. Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: AMO PUERTO RICO MFG. INC..
- Total reports
- 11,598
- Deaths
- 0
- Injuries
- 3,923
- Malfunctions
- 7,675
Reports per year
420
1,86021
1,99322
2,18523
2,23024
2,16025
1,16626
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Intraocular LensHQL9,082
- Lens, Intraocular, Toric OpticsMJP1,229
- Lens, Multifocal IntraocularMFK712
- Extended Depth Of Focus Intraocular LensPOE316
- Lens, Guide, IntraocularKYB254
- Drills, Burrs, Trephines & Accessories (Compound, Powered)HBF2
- Instrument, Vitreous Aspiration And Cutting, Battery-PoweredHKP1
- Unit, PhacofragmentationHQC1
- Device, Irrigation, Ocular SurgeryKYG1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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