PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: May 17, 2017 Initiated: April 20, 2017 #D-0697-2017

Product Description

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

Reason for Recall

Product is being recalled due to low pH value.

Details

Recalling Firm
Akorn, Inc.
Units Affected
1,292 kits
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product 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. Recalled by Akorn, Inc.. Units affected: 1,292 kits.
Why was this product recalled?
Product is being recalled due to low pH value.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 17, 2017. Severity: Low. Recall number: D-0697-2017.