Drugs & medicalClass I

Fresenius Kabi USA, LLC recalls Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only,…

Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.

Read the official notice →
Date
2026-08-26
Country
United States
Brand
Fresenius Kabi
Product
Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only,…
Classification
Class I
Units
Nationwide within the USA.
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Fresenius Kabi recalls

  1. 2026-09-02
  2. US
    Drugs & medicalClass I

    Fresenius Kabi USA, LLC recalls Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA, LLC, Lake Zurich,…

    Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.

    FDA · DrugFresenius Kabi USA, LLCNationwide in the USAOfficial notice →
  3. 2026-07-29
  4. US
    Drugs & medicalClass II

    Fresenius Kabi USA, LLC recalls Naropin (ropivacaine hydrochloride Injection, USP), 0.5%, 100 mg per 20 mL (5 mg per mL), Twenty-five, 20 mL Single-Dose Vials, Rx only,…

    Presence of Particulate Matter: Hair was found in products

    FDA · DrugFresenius Kabi USA, LLCNationwide within in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    Fresenius Kabi USA, LLC recalls Glycopyrrolate Injection, USP, 1 mg per 5 mL (0.2 mg per mL), 25 x 5 mL fill in a 6.5 mL vial, Rx only, Multiple Dose Vials, Fresenius…

    Presence of Particulate Matter: Hair was found in product

    FDA · DrugFresenius Kabi USA, LLCNationwide within in the USAOfficial notice →
  6. 2026-06-17
  7. US
  8. 2026-06-10
  9. US
    Drugs & medicalClass II

    Fresenius Kabi USA, LLC recalls The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.

    Potential for the Cassette Loading Lever to break.

    FDA · DeviceFresenius Kabi USA, LLCUS Nationwide distribution in the states of CA, CO, FL, GA, ID, IL, MA, MD,…Official notice →
  10. US
    Drugs & medicalClass I

    Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004

    Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore…

    FDA · DeviceFresenius Kabi USA, LLCDomestic: CA, CO, FL, GA, ID, IL, MD, MI, MI , MN, MO, MS, NE, NJ, NV, OK, OR,…Official notice →
All 31 Fresenius Kabi recalls →

Other drugs & medical recalls in the United States

  1. 2026-08-26
  2. US
    Drugs & medicalClass II

    Spectral Instruments Inc recalls Lago X

    Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

    FDA · DeviceSpectral Instruments IncUnited States.Official notice →
  3. US
    Drugs & medicalClass I

    Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF: D015251NK, BD Needle…

    After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove…

    FDA · DeviceBard Access Systems, Inc.US: MA, FL, IA, SC, IL, NY, UT, NJ, ID, IN, PA, CA, TX, OH, MO, VA, MD, NC,…Official notice →
  4. US
    Drugs & medicalClass II

    American Regent, Inc. recalls Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a) 10 mL Multi-Dose Vial (NDC…

    Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

    FDA · DrugAmerican Regent, Inc.Nationwide within the U.SOfficial notice →
  5. US
  6. US
    Drugs & medicalClass II

    Golden State Medical Supply Inc. recalls Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count bottles (NDC…

    CGMP deviations: tablets with black specks.

    FDA · DrugGolden State Medical Supply Inc.USA NationwideOfficial notice →
  7. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa…

    CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCUS Nationwide.Official notice →
See all drugs & medical recalls →