FDA recall record

FLUCONAZOLE GREENSTONE BRAND fluconazole for Oral Suspension, ORANGE FLAVORED, 40 mg/mL recall — FDA D-1356-2014

Defective Container: Tamper evident ring failures discovered on some bottles.

Class IIclassification
D-1356-2014official record ID
Jun 11, 2014report date

Recall record at a glance

Official recordD-1356-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPfizer Inc.
Report dateJun 11, 2014
Recall initiation dateJan 29, 2014
Quantity4,155 bottles
LocationNew York, NY, United States

Official product description

GREENSTONE BRAND fluconazole for Oral Suspension, ORANGE FLAVORED, 40 mg/mL, when reconstituted, Rx only, Distributed by Greenstone LLC Peapack, NJ 07977. MADE IN INDIA. NDC 59762-5030-1

Why the product was recalled

Defective Container: Tamper evident ring failures discovered on some bottles.

Distribution information

Nationwide, Italy and Republic of South Korea

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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