March 2026 FDA Recall Magnesium Sulfate by Amneal Pharmaceuticals, Llc
D-0478-2026 - Product mix up

This Class I drug recall was voluntarily initiated by Amneal Pharmaceuticals, Llc on March 18, 2026 for the product Magnesium Sulfate. The FDA reported the reason for recall as product mix up. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0478-2026

Reason for Recall
Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.
Initiated
03-18-2026
Reported
04-08-2026
Quantity
784 (12x100mL) cartons

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Amneal Pharmaceuticals, LLC
Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad, 382110, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1720-3.

Batch or Lot Expiration Information

Lot# Lot: AH250162, Exp 8/31/2027