Class II
Terminated
LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12
- Company
- Akorn, Inc.
- Recall Initiated
- March 17, 2017
- Posted
- April 19, 2017
- Recall Number
- D-0661-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 107,940 bottles
- Firm Location
- Lake Forest, IL, United States
Reason for Recall
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Distribution
Nationwide
Lot / Code Info
Lot # LAB15G52, LAB11G52, Exp 6/17; LAB18I52, Exp 8/17; LAB9L52, 11/17; LAB1A62, LAB9A62, Exp 12/17
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