PF-Succinylcholine Chloride Injection — Class III drug recall D-0154-2020
Terminated recall by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center, reported 2019-11-06, distributed nationwide. Incorrect labeling: Incorrect or missing lot and/or exp date
| Recall number | D-0154-2020 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center, West Columbia, SC, United States |
| Recall initiated | 2019-10-21 |
| Classified | 2019-10-28 |
| Reported by FDA | 2019-11-06 |
| Terminated | 2020-05-07 |
| Distributed | Nationwide (US) |
| Quantity | 19,390 syringes |
| Reason classes | labeling |
| NDC | 69374-0919-10 |
| Lot numbers | SU9079A, SU9079B |
| Expiration dates | 2020-04-05 |
Product
PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B Outsourcing Facility 4500 12th St. Ext West Columbia, SC 29172, NDC 69374-919-10.
Reason for recall
Incorrect labeling: Incorrect or missing lot and/or exp date
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-0154-2020. 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.