Laseredge 1 — Class II medical device recall Z-2365-2019
Terminated recall by Bausch & Lomb Inc Irb, reported 2019-09-04, distributed nationwide. Possible dull knife edge
| Recall number | Z-2365-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bausch & Lomb Inc Irb, Rochester, NY, United States |
| Recall initiated | 2016-07-11 |
| Classified | 2019-08-23 |
| Reported by FDA | 2019-09-04 |
| Terminated | 2019-08-30 |
| Distributed | Nationwide (US) |
| Lot numbers | MAWS530, MAXA950 |
| Model numbers | E7592 |
Product
Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Reason for recall
Possible dull knife edge
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-2365-2019. 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.