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

FDA recall notice · announced May 17, 2017 · Akorn

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The 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

Reason for recall

Product is being recalled due to low pH value.

Notes

Distribution: Nationwide
Lot/code information: Kit Lot #031126; Exp 8/2018
Quantity: 1,292 kits
Status: Terminated
Products in this recall event:
- 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 (D-0697-2017)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.