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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug

Central Admixture Pharmacy Services, Inc.: Non Sterility; microbial contamination identified as Aspergillus species

Agency Publication Date: August 25, 2014
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Affected Products

Product: PEDIATRIC CARDIOPLEGIA, 255 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Lot # 13-920741-0-1 EXP 21 JUN 2014

Lot Numbers:
13-920741-0-1
Product: del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Lot# 13-920742-0-1 EXP 21 JUN 2014 and Lot# 13-920452-0-1 through 13-920452-0-30, EXP 21 JUN 2014

Lot Numbers:
13-920742-0-1
13-920452-0-1
Product: adenosine 90 mg in 0.9% sodium chloride/90 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Lot# 13-920757-0-1 through Lot# 13-920757-0-5 (5 total doses) EXP 06 JUL 2014

Lot Numbers:
13-920757-0-1
13-920757-0-5
Product: LOW Potassium Cardioplegia 792 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Lot # 13-920739-01 through Lot # 13-920739-04 (4 total doses) EXP 21 Jun 2014

Lot Numbers:
13-920739-01
13-920739-04

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 68532
Status: Resolved
Manufacturer: Central Admixture Pharmacy Services, Inc.
Manufactured In: United States
Units Affected: 4 products (1 dose; 31 doses; 5 doses; 4 doses)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.