Could cause temporary or reversible harm; serious harm is unlikely.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
| Distributed by / for | Central Admixture Pharmacy Services, Inc. |
| NDC | 72196-0202-1 |
| Full product label | Cardioplegia Solution del Nido Formula, Total Volume = 1,052.8 mL, EVA Bag, PLASMA-LYTE A 1000 mL, Mannitol 20% 16.3 mL, Sodium Bicarbonate 8.4% 13 mL, Potassium Chloride 2 mEq/mL 13 mL, Magnesium Sulfate 4.06 mEq/mL 4 mL, Lidocaine 2% 6.5 mL, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-0202-1 |
| Recalling firm | Central Admixture Pharmacy Services, Inc. |
| Distribution | Nationwide in the USA |
| Quantity | 786 Bags |
| Recall initiated | 2023-08-17 |
| Report date | 2023-09-06 |
| Recall completed | 2025-03-27 |
| Recall number | D-1112-2023 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Phoenix AZ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗