Class III · Low riskTerminated Initiated Mar 29, 2018 (8 years ago)
Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cups (NDC 50383-720-15)…
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
What was recalled
Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cups (NDC 50383-720-15) packaged in 100-count (10 x 10) cups per case pack (NDC 50383-720-18 or 50383-720-19), Rx Only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701.
Recalling firm
Akorn, Inc.
NDC code
50383-720-15
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0611-2018
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.