Reported Sep 23, 2015 · Terminated
Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx…
Hospira Inc.
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. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only
- Manufactured byHospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05
- Lot codes and dates
Lot #s: 43406DDExp 7/1/201644255DDExp 8/1/2016
- Amount recalled
- 83,320 vials
Where it was sold
- Nationwide
Why it was recalled
Defective Container: There were customer complaints of cracked and leaking glass vials.
This product could cause temporary or reversible health problems — stop using it.
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