del Nido Cardioplegia Solution — Class II drug recall D-0151-2020
Terminated recall by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center, reported 2019-10-30, distributed nationwide. Lack of Assurance of Sterility; bags have potential to leak
| Recall number | D-0151-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center, West Columbia, SC, United States |
| Recall initiated | 2019-10-09 |
| Classified | 2019-10-18 |
| Reported by FDA | 2019-10-30 |
| Terminated | 2020-12-01 |
| Distributed | Nationwide (US) |
| Quantity | 1,047 bags |
| Reason classes | sterility, packaging |
| NDC | 69374-0984-10 |
| Lot numbers | NC9048A, NC9048B, NC9049A, NC9049B, NC9051A, NC9051B, NC9052A, NC9052B, NC9053A, NC9053B, NC9054A, NC9054B, NC9055A, NC9056B |
| Expiration dates | 2019-10-14, 2019-10-16, 2019-10-21, 2019-10-22, 2019-10-23, 2019-10-28, 2019-10-30, 2019-11-04 |
Product
del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10
Reason for recall
Lack of Assurance of Sterility; bags have potential to leak
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-0151-2020. 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.