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.

EPINEPHrine 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi Compounding, LLC Due to cGMP violations

Date: September 25, 2024
Company: Fresenius Kabi Compounding, LLC
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 Fresenius Kabi Compounding, LLC directly.

Affected Products

EPINEPHrine 0.9% Sodium Chloride Injection USP, 8 mg per 250 mL Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-060-58

Quantity: 753 bags

Why Was This Recalled?

cGMP violations

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Fresenius Kabi Compounding, LLC

Fresenius Kabi Compounding, LLC has 15 total recalls tracked by RecallDetector.

Related Recalls

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