Bausch + Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
Bausch + Lomb is voluntarily recalling 1,236,749 LaserEdge ophthalmic knives because of an atypical volume of complaints regarding dull blades.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is a voluntary precautionary measure initiated due to quality control issues (dull blades) without reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Bausch + Lomb Inc Irb is voluntarily recalling 1,236,749 units of LASEREDGE Knives, specifically the KNIFE ANGLED BEVELED UP 2.7 (6/BOX) with REF/PRODUCT CODE E7559A. These sterile, prescription-only surgical instruments are intended for use in ophthalmic surgery. The recall covers products manufactured without electro-polish control and penetration force testing.
The recall was initiated after the company's complaints database was reviewed, revealing an atypical volume of complaints regarding dull blades for various lots. As a precautionary measure, the manufacturer is recalling all product codes manufactured without the specified quality controls.
The affected products were distributed nationwide in the United States. Because these are prescription-only medical devices intended for professional surgical use, consumers are not expected to possess these items. Healthcare facilities and surgical providers should stop using the affected knives and contact the manufacturer for instructions on return or replacement.
The recalled product
- Product
- LASEREDGE Knives, KNIFE ANGLED BEVELED UP 2.7(6/BOX), REF/PRODUCT CODE E7559A, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
- Manufacturer
- Bausch & Lomb Inc Irb
- Affected units
- 1,236,749
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- none
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 44 recalled by Bausch & Lomb Inc Irb under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 44 products in this recall →Related recalls
Same manufacturer · Bausch & Lomb Inc Irb
See all →- ModerateBausch & Lomb Recalls Laseredge Knives Due to Possible Dull Edge
FDA (Devices) · 2019-09-04
- ModerateBausch & Lomb Recalls Laseredge 1.1mm Arrow Knife Due to Dull Edge
FDA (Devices) · 2019-09-04
- ModerateBausch + Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
FDA (Devices) · 2018-03-14
- ModerateBausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
FDA (Devices) · 2018-03-14
- ModerateBausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
FDA (Devices) · 2018-03-14
Same hazard · dull blade
See all →- HighAlcon ophthalmic surgical knives recalled for sharpness defects
FDA (Devices) · 2024-08-28
- HighSX-One MicroKnife Recalled for Potential Dull Blade Defect
FDA (Devices) · 2022-07-27
- ModerateBausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
FDA (Devices) · 2018-03-14
- ModerateBausch + Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
FDA (Devices) · 2018-03-14
- ModerateBausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
FDA (Devices) · 2018-03-14