PZKClass 3
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA adverse event reports and recall history for light adjustable lens (lal) and light delivery device (ldd) (product code PZK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,311
- Deaths
- 0
- Injuries
- 1,307
- Malfunctions
- 4
Reports per year
1820
8821
7722
12123
26024
44625
30126
Source: FDA adverse event reports by year received, 2020–2026. 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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