The Magnesium Sulfate Injection Recall was announced on March 24, 2026, after Amneal Pharmaceuticals said one lot of Magnesium Sulfate in Water for Injection, USP, may contain the wrong IV bag. According to the FDA notice, a pouch labeled for magnesium sulfate was found to contain Tranexamic Acid in 0.7% Sodium Chloride Injection instead. Because this product was distributed nationwide to wholesalers and distributors and recalled to the hospital level, the Magnesium Sulfate Injection Recall is an important safety alert for hospitals, healthcare workers, and patients who may have recently received IV treatment.
This recall is important because the medication involved is commonly used in hospitals for critical treatments, including pregnancy complications and seizure prevention.
What Is the Magnesium Sulfate Injection Recall?
Product Name: Magnesium Sulfate in Water for Injection, USP
Strength: 4g/100mL
Container: IV Bag
Company: Amneal Pharmaceuticals LLC
Distribution: Nationwide (United States)
This product was distributed to hospitals and medical providers across the country.
Why the Magnesium Sulfate Injection Recall Was Issued
The recall was issued because a Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid. That means the outside packaging and the medication inside did not match. This kind of product mix-up matters because patients could receive the wrong drug if the issue is not caught before administration. Amneal said the chance of the mix-up reaching a patient is considered low because hospitals use multiple medication safety checks, and the Tranexamic Acid IV bag is clearly labeled and barcoded.
Which Product Is Affected by the Magnesium Sulfate Injection Recall?
The recalled product is:
- Product: Magnesium Sulfate in Water for Injection, USP
- Strength: 4g/100mL
- Form: IV bag
- NDC: 70121-1720-3
- Lot: AH250162
- Company: Amneal Pharmaceuticals LLC
The FDA page says the product was packaged 12 x 100mL pouches per carton and distributed nationwide.
Why the Magnesium Sulfate Injection Recall Is Serious
This Magnesium Sulfate Injection Recall is serious because magnesium sulfate is indicated for the prevention and control of seizures in preeclampsia and eclampsia. The FDA notice warns that a delay in receiving magnesium therapy could lead to life-threatening or long-term morbidity in pregnant individuals with preeclampsia or eclampsia, and could also create risks for preterm neonates because of complications of prematurity. If Tranexamic Acid is given by mistake, potential adverse events include blood clotting, seizures, hypersensitivity reactions, visual disturbances, and dizziness. Amneal said it had not received any adverse event reports related to this recall as of the announcement date.
Where the Product Was Distributed
The recalled medication was distributed nationwide to hospitals and medical facilities, not typically sold directly to consumers or pharmacies.
However, patients who recently received IV treatment in a hospital may want to be aware of this recall.
What Hospitals Should Do After the Magnesium Sulfate Injection Recall
Amneal said hospitals that have the recalled Magnesium Sulfate in Water for Injection should stop using it and return it. The company is notifying distributors and asking them to notify hospital customers. Hospitals with questions can contact Amneal at 833-582-0812 Monday through Friday, 8:00 a.m. to 5:00 p.m. EST, or by email at MagnesiumSulfateRecall@amneal.com. The FDA also says adverse reactions or quality problems may be reported through MedWatch.
Hospitals and medical providers have been notified and are removing affected products.
You can read the official FDA recall announcement here:
This recall was announced by the FDA, and the official recall notice can be viewed on the FDA website. https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-voluntary-nationwide-recall-magnesium-sulfate-water-injection-usp
You can view more recent safety alerts and product recalls on our Consumer Safety Alerts page. https://everydayanswers.online/category/consumer-safety/appliance-recalls/
Final Thoughts on the Magnesium Sulfate Injection Recall
The Magnesium Sulfate Injection Recall is not a typical household recall, but it is still an important safety alert because it involves a hospital-use medication and a product mix-up that could delay proper treatment. Patients who were recently treated in a hospital and have concerns can contact the facility where care was received and ask whether the recalled product was involved. For official recall details, lot information, and company contact instructions, readers should review the FDA notice directly.
Recall Safety Reminder
Recalls happen more often than people realize, and many products are recalled after they have already been distributed nationwide. Always pay attention to recall announcements and check products in your home regularly. Sharing recall information can help protect friends and family.