Low Potassium Cardioplegia (Central Admixture) – microbial contamination (2014)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LOW Potassium Cardioplegia 792 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
Brand
Central Admixture Pharmacy Services, Inc.
Lot Codes / Batch Numbers
Lot # 13-920739-01 through Lot # 13-920739-04 (4 total doses) EXP 21 Jun 2014
Products Sold
Lot # 13-920739-01 through Lot # 13-920739-04 (4 total doses) EXP 21 Jun 2014
Central Admixture Pharmacy Services, Inc. is recalling LOW Potassium Cardioplegia 792 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 4 due to Non Sterility; microbial contamination identified as Aspergillus species. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Non Sterility; microbial contamination identified as Aspergillus species
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
MI, WI
Page updated: Jan 10, 2026