Akorn, Inc. recalls IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized pow…

Recall date

April 20, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0697-2017

FDA classification

Class III

Brand / firm

Akorn, Inc.

Sold / distributed

Nationwide

Why it was recalled

Product is being recalled due to low pH value.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized powder, Rx only, Manufactured by: Akorn, Inc., NDC 17478-701-02