FDA recall record

CIPLA Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle recall — FDA D-1498-2022

Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could…

Class IIclassification
D-1498-2022official record ID
Sep 14, 2022report date

Recall record at a glance

Official recordD-1498-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCIPLA
Report dateSep 14, 2022
Recall initiation dateAug 22, 2022
Quantity3,468 bottles
LocationWarren, NJ, United States

Official product description

Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle, RX only, Manufactured for Exelan Pharmecuticals, Inc., Boca Raton, FL 33432, NDC 76282-708-50.

Why the product was recalled

Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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