PSA DROP — 03/24/2026
Bridgewater, New Jersey

Yo, listen up — Amneal Pharmaceuticals is steppin’ to the mic with an important recall alert. One batch of Magnesium Sulfate in Water for Injection, USP, 4g/100mL IV bags got mixed up in the lineup.
Somebody cracked open a pouch and found Tranexamic Acid in 0.7% Sodium Chloride Injection, 10 mg/mL chillin’ where the magnesium was supposed to be.

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⚠️ THE REAL TALK — RISK BREAKDOWN
If a patient who needs magnesium — especially pregnant folks dealing with preeclampsia or eclampsia — doesn’t get it on time, that delay can be dangerous. We’re talkin’ seizures, long‑term complications, and serious risks for preterm babies too.

Ain’t no reports of harm so far, but if TXA gets pumped in by accident, it can bring its own problems:

• Blood clots
• Seizures
• Allergic reactions
• Vision issues
• Dizziness

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📦 THE PRODUCT IN QUESTION

• Magnesium Sulfate in Water for Injection
  NDC: 70121‑1720‑3
  Lot: AH250162
  Packed 12 pouches per carton
  Shipped nationwide between 12/22/2025 – 2/27/2026
• Tranexamic Acid in 0.7% Sodium Chloride
  Usually used short‑term for folks with hemophilia to keep bleeding in check during tooth extractions.

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🔍 HOW LIKELY IS THE MIX‑UP?
Low. Hospitals run multiple safety checks before anything hits a patient’s IV line.
Amneal already inspected 74% of the magnesium pouches they still had — no other mix‑ups spotted.
Plus, every TXA bag is clearly labeled and bar‑coded, so the wrong bag sticks out like a fake chain.

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📢 WHAT HOSPITALS NEED TO DO
If you’ve got the recalled Magnesium Sulfate on deck:
Stop using it. Send it back.

Return to:
Amneal Pharmaceuticals
Magnesium Sulfate Recall Coordinator
21 Colonial Drive
Piscataway, NJ 08854

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☎️ QUESTIONS? HIT THEM UP
Phone: 833‑582‑0812 (Mon–Fri, 8 AM–5 PM EST)
Fax: 631‑983‑2595
Email: MagnesiumSulfateRecall@amneal.com

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📝 REPORTING ISSUES TO THE FDA
If you catch any reactions or quality problems, drop a report through MedWatch:

Online: http://www.fda.gov/medwatch/report.htm
Mail/Fax: Grab the form at http://www.fda.gov/MedWatch/getforms.htm or call 1‑800‑332‑1088
Fax completed forms to 1‑800‑FDA‑0178

This recall is fully on the FDA’s radar.

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🎧 Consumer Contact
Amneal Pharmaceuticals
833‑582‑0812