RecallRadar

FDA Drug recall D-0418-2026

Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), R…

On 2026-04-01 the FDA classified a Class II recall of Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), R… by Amerisource Health Services, citing failed tablet specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0418-2026
ClassificationClass II
Statusongoing
Initiated2026-03-16
Published2026-04-01
Last updated2026-09-13 11:52 UTC
CompanyAmerisource Health Services
DistributionUS

Product

Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.

Reason

Failed tablet specifications.

Identifiers

ndc60687-775-11
ndc60687-775-01
ndc60687-775-65
ndc60687-730-11
ndc60687-730-01
ndc60687-730-65
code_infoLot #1024852; Exp 9/30/2026

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0418-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.