FDA recall record

Akorn Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton recall — FDA D-1241-2019

Failed impurities/degradation specification: Out of Specification result for total impurity at 4.0% (Limit: NMT 3.0%) at 12 months stability testing.

Class IIIclassification
D-1241-2019official record ID
May 1, 2019report date

Recall record at a glance

Official recordD-1241-2019
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAkorn Inc.
Report dateMay 1, 2019
Recall initiation dateApr 23, 2019
Quantity5,380 cartons (25 ampules per carton)
LocationLake Forest, IL, United States

Official product description

Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-25

Why the product was recalled

Failed impurities/degradation specification: Out of Specification result for total impurity at 4.0% (Limit: NMT 3.0%) at 12 months stability testing.

Distribution information

U.S.A. Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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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