FDAFDA · Food and drugs·Recall number D-0856-2021
Morphine Sulfate Injection, USP, 2 mg per mL, 1 mL single dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-452-01. 25 vials per tray packaged 18 trays per shipper
Published October 6, 2021 · Recall initiated: September 17, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Defective container: Cracked vials leading to lack of sterility assurance
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- MORPHINE SULFATE
- Manufacturer
- Fresenius Kabi USA LLC
- Distributor
- U.S.A. Nationwide
- UPC
- 0363323454005
- Lot
- Lot # 6023731, 6023732, Exp 03/2023; 6024172, 6024260, Exp 06/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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