Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

del Nido Cardioplegia Solution Recalled by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center Due to Lack of Assurance of Sterility; bags have potential...

Date: October 9, 2019
Company: Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center directly.

Affected Products

del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10

Quantity: 1047 bags

Why Was This Recalled?

Lack of Assurance of Sterility; bags have potential to leak

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center has 6 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report