FDA recall record

Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL) 2 mL Single-dose Fliptop Vials recall — FDA D-1446-2020

Lack of Assurance of Sterility; potential loose metal overseal crimp defects.

Class IIclassification
D-1446-2020official record ID
Aug 12, 2020report date

Recall record at a glance

Official recordD-1446-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPfizer Inc.
Report dateAug 12, 2020
Recall initiation dateJul 20, 2020
Quantity19,144 vials
LocationNew York, NY, United States

Official product description

Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL) 2 mL Single-dose Fliptop Vials, Rx only, Distributed by Hospira, Inc. Lake Forest, IL 60045 USA NDC 0409-9094-12

Why the product was recalled

Lack of Assurance of Sterility; potential loose metal overseal crimp defects.

Distribution information

United States including Puerto Rico

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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