US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 20, 2020 (6 years ago)

Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL) 2 mL Single-dose Fliptop…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Pfizer Inc.
NDC code
0409-9094-12
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1446-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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