Reported Apr 19, 2017 · Terminated
LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn,…
Akorn, 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: Akorn, Inc. · 1925 W Field Ct Ste 300 · Lake Forest, IL · 60045-4862
Is this the product you have?
LATANOPROST OPHTHALMIC SOLUTION0.005%125 ug/2.5 mLpackaged in 2.5 mL bottleRx only
- Manufactured forAkorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12
- Lot codes and dates
Lot # LAB15G52LAB11G52Exp 6/17LAB18I52Exp 8/17LAB9L5211/17LAB1A62LAB9A62Exp 12/17
- Amount recalled
- 107,940 bottles
Where it was sold
- Nationwide
Why it was recalled
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
This product could cause temporary or reversible health problems — stop using it.
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