The Recall Desk

FDA (Devices) recall action 74671

Bausch & Lomb Inc Irb recalled 2 products on 2019-09-04

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2019-09-04
Critical
0
Units
—

Why these products were recalled

Possible dull knife edge

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • ModerateFDA (Devices)··2019-09-04

    Bausch & Lomb Recalls Laseredge 1.1mm Arrow Knife Due to Dull Edge

    Bausch & Lomb is recalling Laseredge 1.1mm Arrow Knives used in ophthalmic surgery because the knife edge may be dull.

    Product
    Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2019-09-04

    Bausch & Lomb Recalls Laseredge Knives Due to Possible Dull Edge

    Bausch & Lomb is recalling specific Laseredge Knives used in ophthalmic surgery because they may have dull edges.

    Product
    Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED, REF E7599 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
    Category
    Distribution
    0 states