FDA recall record

Akorn Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL Unit Dose Cup, a) unit dose cup recall — FDA D-1088-2017

Crystallization with subpotent out of specification assay results for chlorhexidine.

Class IIIclassification
D-1088-2017official record ID
Aug 23, 2017report date

Recall record at a glance

Official recordD-1088-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAkorn Inc.
Report dateAug 23, 2017
Recall initiation dateJul 12, 2017
Quantity541,900 unit dose cups (5,419 trays)
LocationLake Forest, IL, United States

Official product description

Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL Unit Dose Cup, a) unit dose cup (NDC 50383-720-15), b) 100-count tray (NDC 50383-720-19), Rx Only, Hi-Tech Pharmacal Co. Inc., Amityville, NY 11701.

Why the product was recalled

Crystallization with subpotent out of specification assay results for chlorhexidine.

Distribution information

Nationwide in the USA

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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