Bausch & Lomb Inc Irb: Medical Device Recall in 2019 - (Recall #: Z-2365-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.

Product Classification:

Class II

Date Initiated: July 11, 2016

Date Posted: September 4, 2019

Recall Number: Z-2365-2019

Event ID: 74671

Reason for Recall:

Possible dull knife edge

Status: Terminated

Product Quantity: 384 packs/6 blades (2,304 individual blades)

Code Information:

Lot Numbers: MAWS530 MAXA950 Expiry Dates: 01-2021

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated