Data Foundry

Medical device recalls 2025

Intraocular lens — Class I medical device recall Z-1679-2025

Ongoing recall by Bausch & Lomb Surgical, Inc., reported 2025-05-14, distributed nationwide. In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with im

Recall numberZ-1679-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBausch & Lomb Surgical, Inc., Clearwater, FL, United States
Recall initiated2025-03-27
Classified2025-05-02
Reported by FDA2025-05-14
DistributedNationwide (US)
Quantity236,840
UPC / GTIN / UDI-DI10757770607072, 10757770607089, 10757770607096, 10757770607102, 10757770607119, 10757770607126, 10757770607492, 10757770607515, 10757770607539, 10757770607553, 10757770607577, 10757770607591, 10757770607614, 10757770607638, 10757770607652, 10757770607676, 10757770607683, 10757770607690, 10757770607706, 10757770607713, 10757770607720, 10757770607737, 10757770607744, 10757770607751, 10757770607768 and 475 more

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;

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1679-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.