LWLClass 3
Fluid, Intraocular
FDA adverse event reports and recall history for fluid, intraocular (product code LWL), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 222
- Deaths
- 3
- Injuries
- 189
- Malfunctions
- 14
Reports per year
612
113
314
315
1316
317
618
219
720
1221
1322
1823
1624
2725
1726
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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