Akorn, Inc. recalls IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized powd
Recalled May 17, 2017 · FDA recall D-0697-2017 · Akorn
Hazard
Product is being recalled due to low pH value. · FDA Class III
Units
1,292 kits
Sold at
Nationwide
Description
Product is being recalled due to low pH value.
Product
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
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →