IC-Green — Class III drug recall D-0697-2017
Terminated recall by Akorn, Inc., reported 2017-05-17, distributed nationwide. Product is being recalled due to low pH value.
| Recall number | D-0697-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Akorn, Inc., Lake Forest, IL, United States |
| Recall initiated | 2017-04-20 |
| Classified | 2017-05-09 |
| Reported by FDA | 2017-05-17 |
| Terminated | 2019-02-21 |
| Distributed | Nationwide (US) |
| Quantity | 1,292 kits |
| NDC | 17478-0701-02 |
| Lot numbers | 031126 |
| Expiration dates | 2018-08 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0697-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.