---
title: "Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further... — FDA record D-0478-2026 | Is It on Recall"
description: "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."
url: https://isitonrecall.com/recall/fda-drug-d-0478-2026-magnesium-sulfate-in-water-for-injection-4g-100-ml-40mg-ml-iv-bag-further-packaged-in-cartons-of-12/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV b... — FDA record D-0478-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 18, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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.
- **Reason**: 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.
- **Classification**: Class I
- **Recalling firm**: Amneal Pharmaceuticals, LLC
- **Quantity**: 784 (12x100mL) cartons
- **Agency-reported status**: Ongoing
- **Source record identifier**: D-0478-2026

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0478-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot: AH250162, Exp 8/31/2027 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.A. Nationwide

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Apr 8, 2026
- **Recall initiation date**: Mar 18, 2026
- **Center classification date**: Apr 13, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0478-2026%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Amneal Pharmaceuticals, LLC records](https://isitonrecall.com/brand/amneal-pharmaceuticals-llc/)
