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enVista MX60 IOL
Bausch & Lomb Incorporated · Model MX60UT125+255 · UDI-DI 10757770540331
NAA
Prescription
0
510(k) clearances
1,402
Adverse events
1
Recalls
4
Facilities
Description
MX60UT125 12.5MM +25.50
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-11-14 | Bausch and Lomb, Incorporated | Bausch + Lomb voluntary initiated the recall due to a physician complaint of haze on the Crystalens AO which was visualized using an angled beam from a slit lamp during the post-op |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.