Recall Z-2365-2019— Bausch & Lomb Inc Irb

Name: FDA recall Z-2365-2019
Creator: U.S. Food and Drug Administration
Published: 2016-07-11

Class II · Terminated

Class II FDA medical device recall by Bausch & Lomb Inc Irb, initiated 2016-07-11, terminated 2019-08-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.. Reason: Possible dull knife edge.

Recalling firm: Bausch & Lomb Inc Irb
Classification: Class II
Status: Terminated
Initiated: 2016-07-11
Terminated: 2019-08-30
Firm location: Rochester, NY, United States

Product description

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

Reason for recall

Possible dull knife edge

Data sourced from openFDA. This site is unofficial and independent of the FDA.