FDA Drug recall D-1560-2014
del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
- FDA Drug
- Class I
- terminated
- Published 2014-09-03
On 2014-09-03 the FDA classified a Class I recall of del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150 by Central Admixture Pharmacy Services, citing non Sterility; microbial contamination identified as Aspergillus species.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1560-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-05-28 |
| Published | 2014-09-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Central Admixture Pharmacy Services |
| Distribution | MI, WI |
Product
del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
Reason
Non Sterility; microbial contamination identified as Aspergillus species
Identifiers
| code_info | Lot# 13-920742-0-1 EXP 21 JUN 2014 and Lot# 13-920452-0-1 through 13-920452-0-30, EXP 21 JUN 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-1560-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.