Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center Due to Incorrect labeling: Incorrect or missing lot and/or exp...
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-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B Outsourcing Facility 4500 12th St. Ext West Columbia, SC 29172, NDC 69374-919-10.
Quantity: 19,390 syringes
Why Was This Recalled?
Incorrect labeling: Incorrect or missing lot and/or exp date
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