Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Recalled by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center Due to GMP Deviations: potential glass contamination
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
PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Sodium Chloride Injection-250 mL Total Dose: (500 mcg/156.3 mg)/250 mL, Rx Only, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC 69374-0525-25
Quantity: 1855 bags
Why Was This Recalled?
GMP Deviations: potential glass contamination
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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