Is Fresenius Kabi USA, LLC recalled?

Yes — a recall has been published. Reason: Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.

SeriousFDAOngoing

Can cause serious harm or death. Speak to your pharmacist or doctor before taking it — do not stop a prescribed medicine on your own.

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

Check the label for

Lot #: 6402820, Exp. Date 12/2028

Why: Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
Distributed: Nationwide within the USA.
Company: Fresenius Kabi USA, LLC
Announced: 26 August 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 4 August 2026

Already ate or took it and feel unwell? Call Poison Control — 1-800-222-1222

Source: FDA record D-0788-2026 · retrieved 24 August 2026

Read the official notice

Every recall is shown word for word from the FDA and USDA, with a link to the source.