FDA recall record

Akorn Halyard 24-Hour Oral Care Kit q2, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine recall — FDA D-1089-2017

Crystallization with subpotent out of specification assay results for chlorhexidine.

Class IIIclassification
D-1089-2017official record ID
Aug 23, 2017report date

Recall record at a glance

Official recordD-1089-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAkorn Inc.
Report dateAug 23, 2017
Recall initiation dateJul 12, 2017
Quantity40,978 unit dose cups
LocationLake Forest, IL, United States

Official product description

Halyard 24-Hour Oral Care Kit q2, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97012

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

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About this record

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