Reported Nov 25, 2015 · Terminated
RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Akorn, Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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: Akorn, Inc. · 1925 W. Field Court, Suite 300 · Lake Forest, IL · 60045
Is this the product you have?
- RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd
- forAkorn, Inc., Lake Forest, IL 60045
- NDC17478-151-42
- Lot codes and dates
- Lot #: 14RIF1(A)
- Expiry9/30/2016
- Amount recalled
- 6861 Vials
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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