FDA Drug recall D-1157-2014
Photofrin (porfimer sodium) for Injection, 75 mg Single Use Flip-Top Vial, Rx Only
- FDA Drug
- Class III
- terminated
- Published 2014-03-19
On 2014-03-19 the FDA classified a Class III recall of Photofrin (porfimer sodium) for Injection, 75 mg Single Use Flip-Top Vial, Rx Only by Pinnacle Biologics, citing stability Data Does Not Support Expiry: Printed expiration date should be Nov 2013 rather than Nov 2014.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1157-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-02-10 |
| Published | 2014-03-19 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Pinnacle Biologics |
| Distribution | US |
Product
Photofrin (porfimer sodium) for Injection, 75 mg Single Use Flip-Top Vial, Rx Only. Manufactured for: Pinnacle Biologics, Inc. Bannockburn, IL 60015. NDC:76128-155-75
Reason
Stability Data Does Not Support Expiry: Printed expiration date should be Nov 2013 rather than Nov 2014.
Identifiers
| ndc | 76128-155-75 |
|---|---|
| code_info | Lot Number: 0M396; Expiry: Nov 2014 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1157-2014%22
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