Bausch & Lomb Inc Irb: Medical Device Recall in 2018 - (Recall #: Z-0883-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: March 3, 2017

Date Posted: March 14, 2018

Recall Number: Z-0883-2018

Event ID: 76874

Reason for Recall:

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Status: Terminated

Product Quantity: 1,236,749 knives in total

Code Information:

none

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated