del Nido Cardioplegia Solution 1000 mL — Class II drug recall D-1269-2022
Terminated recall by Nephron Sterile Compounding Center LLC, reported 2022-07-27, distributed nationwide. Lack of Assurance of Sterility
| Recall number | D-1269-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nephron Sterile Compounding Center LLC, West Columbia, SC, United States |
| Recall initiated | 2022-06-30 |
| Classified | 2022-07-18 |
| Reported by FDA | 2022-07-27 |
| Terminated | 2024-06-17 |
| Distributed | Nationwide (US) |
| Quantity | 1,765 bags |
| Reason classes | sterility |
| NDC | 69374-0984-10 |
| Lot numbers | NC2031A, NC2033A, NC2034A, NC2035A |
| Expiration dates | 2022-07-07, 2022-07-12, 2022-07-18, 2022-07-19 |
Product
del Nido Cardioplegia Solution 1000 mL (1000 mL) Single-Dose Container IV bag, 4 x 1 IV Bag per case, 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
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-1269-2022. 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.