United StatesMorphine Sulfate Injection, USP 2 mg/mL in 1 mL single‑dose Simplist prefilled syringes (Unit of Use NDC 76045-004-01; Unit of Sale NDC 76045-004-11), Lot #6402820, exp. 12/2028, sold nationwide, is being recalled by Fresenius Kabi USA, LLC. The recall is due to a labeling mixup where a MicroVault labeled as Morphine 2 mg/1 mL contains a prefilled syringe of Dilaudid 0.5 mg/0.5 mL; 625,500 syringes are affected.
What's being recalled
Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only, Fresenius Kabi, Lake Zurich, IL. Unit of Use NDC Number 76045-004-01; Unit of Sale NDC Number 76045-004-11
Recalling firm: Fresenius Kabi USA, LLC, Lake Zurich, IL, United States.
How to identify it
Lot #: 6402820, Exp. Date 12/2028
The hazard
Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Nationwide within the USA.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)