FDAFDA · Food and drugs·Recall number D-0136-2020
10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13
Published October 16, 2019 · Recall initiated: October 2, 2019
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
Lack of Assurance of Sterility: Bag has the potential to leak.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LMD IN DEXTROSE
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide in the United States and Puerto Rico
- Lot
- Lot #: 87-095-JT Exp. 1MAR2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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