Reported Jun 21, 2017 · Terminated
Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC…
Hospira Inc., A Pfizer Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira Inc., A Pfizer Company · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04
- Lot codes and dates
720503A720603A (Canada only)
- Amount recalled
- (720503A): 43,200 vials, (720603A): 400 vials
Where it was sold
- Nationwide
Why it was recalled
GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
This product could cause temporary or reversible health problems — stop using it.
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