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
Reported: October 16, 2019 Initiated: October 2, 2019 #D-0136-2020
Product Description
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
Reason for Recall
Lack of Assurance of Sterility: Bag has the potential to leak.
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 17832 bags
- Distribution
- Nationwide in the United States and Puerto Rico
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Pfizer Inc.. Units affected: 17832 bags.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Bag has the potential to leak.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 16, 2019. Severity: Moderate. Recall number: D-0136-2020.
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