Class I ยท High risk
Magnesium Sulfate in Water for Injection
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.
National Drug Code
Is NDC 70121-1720-03 recalled?
Magnesium Sulfate · 12 POUCH in 1 CARTON (70121-1720-3) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
Yes — this exact package was recalled
1 FDA recall names the code 70121-1720-03 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Magnesium Sulfate In Water For
- Strength
- MAGNESIUM SULFATE HEPTAHYDRATE 40 mg/mL
- Form
- Injection · Intravenous
- Labeler
- Amneal Pharmaceuticals LLC
- Type
- Human Prescription Drug
- Product code
- 70121-1720
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 70121-1390 See recall 2
- 70121-1574 Methylprednisolone acetate 1
- 70121-1685 Exenatide 1
- 70121-1734 Ropivacaine Hydrochloride 1
- 70121-2453 Pemrydi Rtu 1
- 70121-2461 Pemrydi Rtu 1
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