FDA recall record

Akorn Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL recall — FDA D-0265-2023

Failed Stability Specifications: Out of specification test results for viscosity was identified at the 12M stability timepoint.

Class IIIclassification
D-0265-2023official record ID
Feb 15, 2023report date

Recall record at a glance

Official recordD-0265-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmAkorn, Inc.
Report dateFeb 15, 2023
Recall initiation dateJan 30, 2023
Quantity45,117 Bottles
LocationGurnee, IL, United States

Official product description

Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02

Why the product was recalled

Failed Stability Specifications: Out of specification test results for viscosity was identified at the 12M stability timepoint.

Distribution information

Nationwide in the USA and Puerto Rico

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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