FDA Medical devices recall ·
Intraocular lens recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-1679-2025
- Date
- (initiated March 27, 2025)
- Company / brand
- Bausch & Lomb Surgical, Inc.
21 N Park Place Blvd, Clearwater, FL, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 236,840
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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;
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Description/Lots/UDI-DI: 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, 3Q26331, 3Q26332, 3Q26333, 3Q26334, 3Q26348, 3Q26422, 3Q26424, 3Q26425, 3Q26444, 3Q26445, 3Q26446, 3Q26520, 3Q26521, 3Q26522, 3Q26614, 3Q26617, 3Q26618, 3Q26681, 3Q26682, 3Q26683, 3Q26684, 3Q26733, 3Q26734, 3Q26735, 3Q26747, 3Q26801, 3Q26802, 3Q26833, 3Q26834, 3Q26835, 3Q26836, 3Q26911, 3Q26912, 3Q26913, 3Q26914, 3Q26916, 3Q27101, 3Q27102, 3Q27103, 3Q27104, 3Q27201, 3Q27202, 3Q27203, 3Q27226, 3Q27253, 3Q27254, 3Q27255, 3Q27336, 3Q27337, 3Q27450, 3Q27451, 3Q27452, 3Q27453, 3Q27454, 3Q27455, 3Q27520, 3Q27620, 3Q27808, 3Q27809, 3Q27928, 3Q27929, 3Q27930, 3Q28021, 3Q28022, 3Q28101, 3Q28137, 3Q28138, 3Q28139, 3Q28712, 3Q28713, 3Q28714, 3Q28812, 3Q28813, 3Q28815, 3Q28816, 3Q28913, 3Q28914, 3Q28915, 3Q29033, 3Q29034, 3Q29140, 3Q29141, 3Q29142, 3Q29215, 3Q29216, 3Q29217, 3Q29218, 3Q29255, 3Q29319, 3Q29320, 3Q29422, 3Q29423, 3Q29424, 3Q29425, 3Q29524, 3Q29526, 3Q29537, 3Q29646, 3Q29647, 3Q29648, 3Q29649
Distribution
Worldwide distribution. US Nationwide including PR and GU, and the countries of CAN, AUS, AUT, BEL, BGR, IC, HRV, CZE, FRA, DEU, GRC, HUN, ITA, NLD, POL, PRT, ROU, ESP, GBR, NZL, HKG.
States: Puerto Rico
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-1679-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.