Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21208 |
| Brand Name: | Laseredge Knife |
| Model: | |
| Affected: | 2.85MM SLIT KNIFE ANG, 6/Box Lots MAYC970, MAYC960, MABX010, MAYL090, 3.0MM SLIT KNIFE ANG BEVUP, 6/Box Lots MAKG600, MAMM950, 1.1MM ARROW KNIFE ANGLED (6/BOX) Lots MAYT510, 1.6MMX1.8MM TRAPEZOLD ANG 6/Box Lots MAXL130, MAWF130, MBRF780 |
| Software version: | |
| Recalling Organisation: | Bausch & Lomb (NZ) Ltd c/o Corporate services New Zealand Level 5, 79 Queen Street Auckland 1010 |
| Contact Information: | |
| Manufacturer: | Bausch & Lomb Inc |
| Issue: | If excessive force is required to push a dull blade through the cornea this may result in a sub-optimal incision. Uncontrolled penetration through the cornea may also result in injury to anterior segment structures. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 13/3/2017 |
