FDA recall record

Imprimis NJOF Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1% recall — FDA D-0547-2024

Lack of Assurance of Sterility

Class IIclassification
D-0547-2024official record ID
Jun 19, 2024report date

Recall record at a glance

Official recordD-0547-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmImprimis NJOF, LLC
Report dateJun 19, 2024
Recall initiation dateMay 14, 2024
Quantity136,005 units
LocationLedgewood, NJ, United States

Official product description

Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1% 5.5mL, Rx Only, This is a compounded drug. NOT FOR RESALE. OFFICE USE ONLY Compounded by: Imprimis NJOF, LLC., 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852 NDC: 71384-514-05

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

US Nationwide

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: N/A.

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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