IC-Green recall
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
Why was IC-Green recalled?
Product is being recalled due to low pH value.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Kit Lot #031126; Exp 8/2018
- 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
- Recalling firm
- Akorn, Inc.
- Quantity
- 1,292 kits
- Distribution
- Nationwide
- Recall date
- May 17, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)