FDA recall record

Akorn Lidocaine 2.5% and Prilocaine Cream, 2.5%. 30g tube recall — FDA D-1046-2018

Failed Impurities/Degredation Specifications: Out of Specification results for an unknown impurity was found during routine stability testing at 12 months.

Class IIclassification
D-1046-2018official record ID
Aug 15, 2018report date

Recall record at a glance

Official recordD-1046-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAkorn, Inc.
Report dateAug 15, 2018
Recall initiation dateAug 1, 2018
Quantity22,605 tubes
LocationLake Forest, IL, United States

Official product description

Lidocaine 2.5% and Prilocaine Cream, 2.5%. 30g tube, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701, NDC 50383-667-30

Why the product was recalled

Failed Impurities/Degredation Specifications: Out of Specification results for an unknown impurity was found during routine stability testing at 12 months.

Distribution information

Nationwide within the USA

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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