Reported May 14, 2025 · Ongoing

Intraocular lens. enVista Monofocal IOL, All models starting with EE; enVista Aspire IOL, All models starting with EA;…

Bausch & Lomb Surgical, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bausch & Lomb Surgical, Inc. · 21 N Park Place Blvd · Clearwater, FL · 33759-3917

Is this the product you have?

  • Intraocular lens. enVista Monofocal IOL, All models starting with EE; enVista Aspire IOL, All models starting with EA; enVista Monofocal Toric IOL, All models starting with ETE; enVista Aspire Toric IOL, All models starting with ETA;
Lot codes and dates
  • Description/Lots/UDI-DI

    3,019 of 3,019 codes

    • enVista Monofocal IOL (EEU)/3Q25120
    • 3Q25326
    • 3Q25327
    • 3Q25347
    • 3Q25348
    • 3Q25425
    • 3Q25426
    • 3Q25427
    • 3Q25507
    • 3Q25508
    • 3Q25509
    • 3Q25510
    • 3Q25511
    • 3Q25548
    • 3Q25549
    • 3Q25550
    • 3Q25628
    • 3Q25632
    • 3Q25730
    • 3Q25731
    • 3Q25840
    • 3Q25843
    • 3Q25934
    • 3Q25935
    • 3Q25936
    • 3Q25937
    • 3Q25938
    • 3Q25939
    • 3Q25940
    • 3Q25941
    • 3Q25942
    • 3Q25943
    • 3Q25944
    • 3Q26009
    • 3Q26010
    • 3Q26041
    • 3Q26042
    • 3Q26043
    • 3Q26044
    • 3Q26069
    • 3Q26070
    • 3Q26071
    • 3Q26072
    • 3Q26119
    • 3Q26120
    • 3Q26121
    • 3Q26122
    • 3Q26123
    • 3Q26202
    • 3Q26203
    • 3Q26204
    • 3Q26220
    • 3Q26255
    • 3Q26262
    • 3Q26301
    • 3Q26305
    • 3Q26306
    • 3Q26328
    • 3Q26329
    • 3Q26330
Amount recalled
236,840

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Stop using this product now

In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Bausch & Lomb Surgical, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.