Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
Bausch & Lomb is voluntarily recalling 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 action taken due to product performance 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 LASEREDGE Knives, 2.75MM THIN SLIT ANGLED BEVELED UP (6/BOX)(6/BOX), REF/PRODUCT CODE E7759A. These sterile, prescription-only surgical instruments are intended for ophthalmic surgery. The recall covers 1,236,749 knives distributed nationwide in the United States.
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, Bausch & Lomb is recalling all product codes manufactured without electro-polish control and penetration force testing.
Surgeons and healthcare facilities should stop using the affected knives and contact Bausch & Lomb for further instructions on the recall process.
The recalled product
- Product
- LASEREDGE Knives, 2.75MM THIN SLIT ANGLED BEVELED UP (6/BOX)(6/BOX), REF/PRODUCT CODE E7759A, 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
- Hazard
- 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 · product defect
See all →- SevereShilpa Medicare Recalls Discolored Pemetrexed Injection Vials
FDA (Drugs) · 2026-08-26
- ModerateShilpa Medicare Recalls Discolored PEMRYDI RTU Injection Vials
FDA (Drugs) · 2026-08-26
- ModerateMedline Sterile Water and Saline Bottles Recalled for Leaking Peel-Foil Seals
FDA (Devices) · 2025-05-07
- HighCELL-DYN Ruby hematology analyzer system expiration date validation
FDA (Devices) · 2025-04-30
- HighMedline Procedure Kits with Defective Plastic Syringes Recalled for Safety
FDA (Devices) · 2025-04-02