Data Foundry

Drug recalls 2018

24-HOUR Oral Care q2 Kit with Ballard* Technology — Class III drug recall D-0612-2018

Terminated recall by Akorn, Inc., reported 2018-04-04, distributed nationwide. Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine a

Recall numberD-0612-2018
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAkorn, Inc., Lake Forest, IL, United States
Recall initiated2018-03-29
Classified2018-03-29
Reported by FDA2018-04-04
Terminated2020-04-22
DistributedNationwide (US)
Quantity48,176 units
Reason classespotency, specification failure
NDC50383-0720-15
Lot numbers0202511399, 0202511400, 0202518977, 0202538282, 0202538283, 0202538284, 0202538285, 0202543552, 0202543553, 0202642220, 0202642224, 0202642225, 03/18, 04/18, 05/18, 350836

Product

24-HOUR Oral Care q2 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health, Inc., 5405 Windward Parkway, Alpharetta, GA 30004; Distributed in the USA by Halyard Sales, LLC, Alpharetta, GA 30004, Product 97012.

Reason for recall

Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0612-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.