Class II
Terminated
Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04
- Company
- Hospira Inc., A Pfizer Company
- Recall Initiated
- May 18, 2017
- Posted
- June 21, 2017
- Recall Number
- D-0898-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- (720503A): 43,200 vials, (720603A): 400 vials
- Firm Location
- Lake Forest, IL, United States
Reason for Recall
GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
Distribution
Nationwide, Canada and Singapore
Lot / Code Info
720503A, 720603A (Canada only)
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