PlainRecalls
FDA Drug Moderate Class II Terminated

Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest, IL 60045; NDC 17478-201-15.

Reported: October 9, 2019 Initiated: September 20, 2019 #D-1883-2019

Product Description

Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest, IL 60045; NDC 17478-201-15.

Reason for Recall

Lack of Assurance of Sterility: Out of specification results for container closure test which cannot guarantee the sterility of the product.

Details

Recalling Firm
Akorn, Inc.
Units Affected
60,176 bottles
Distribution
Nationwide in the USA and Puerto Rico
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest, IL 60045; NDC 17478-201-15.. Recalled by Akorn, Inc.. Units affected: 60,176 bottles.
Why was this product recalled?
Lack of Assurance of Sterility: Out of specification results for container closure test which cannot guarantee the sterility of the product.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 9, 2019. Severity: Moderate. Recall number: D-1883-2019.