Medical device recalls Moderate risk

Bausch & Lomb Inc Irb recalls Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical proce…

Recall date
July 11, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2365-2019
FDA classification
Class II
Brand / firm
Bausch & Lomb Inc Irb
Sold / distributed
US Nationwide Distribution

Why it was recalled

Possible dull knife edge

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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