Class II — Bausch & Lomb Inc Irb
| Recalling firm | Bausch & Lomb Incorporated |
|---|---|
| Registered facility | View this company's 10 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Possible dull knife edge |
| Product | Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures. |
| Quantity | 384 packs/6 blades (2,304 individual blades) |
| Distribution | US Nationwide Distribution |
| Initiated | 2016-07-11 |
| Classified | 2019-08-23 |
| Terminated | 2019-08-30 |
| Recall number | Z-2365-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Bausch & Lomb Inc Irb (Z-2365-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74671/
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