FDA Device recall Z-2365-2019
Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures
- FDA Device
- Class II
- terminated
- Published 2019-09-04
On 2019-09-04 the FDA classified a Class II recall of Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures by Bausch And Lomb Irb, citing possible dull knife edge.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2365-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-11 |
| Published | 2019-09-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Bausch And Lomb Irb |
| Distribution | US |
Product
Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Reason
Possible dull knife edge
Identifiers
| code_info | Lot Numbers: MAWS530 MAXA950 Expiry Dates: 01-2021 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2365-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.